chr6:160113872:A>G Detail (hg19) (SOD2)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr6:160,113,872-160,113,872 |
hg38 | chr6:159,692,840-159,692,840 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001322814.1:c.47T>C | NP_001309743.1:p.Val16Ala |
NM_001024466.2:c.47T>C | NP_001019637.1:p.Val16Ala | |
NM_001024465.2:c.47T>C | NP_001019636.1:p.Val16Ala |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:0.111 |
ToMMo:0.122 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:0.160 |
Prediction
ClinVar
Clinical Significance | Conflicting classifications of pathogenicity; risk factor |
Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
![]() |
2007-01-01 | no assertion criteria provided | SUPEROXIDE DISMUTASE 2 POLYMORPHISM |
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Detail |
Likely risk allele; risk factor | 2007-01-01 | no assertion criteria provided | Microvascular complications of diabetes, susceptibility to, 6 |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.129 | liver carcinoma | Six SNPs of five genes (rs1800562 of HFE, rs17868323 and rs11692021 of UGT1A7, r... | BeFree | 21240526 | Detail |
0.017 | liver carcinoma | Six SNPs of five genes (rs1800562 of HFE, rs17868323 and rs11692021 of UGT1A7, r... | BeFree | 21240526 | Detail |
0.030 | liver carcinoma | Six SNPs of five genes (rs1800562 of HFE, rs17868323 and rs11692021 of UGT1A7, r... | BeFree | 21240526 | Detail |
<0.001 | pancreatic carcinoma | According to the assumption that genetic variation in carcinogen metabolism furt... | BeFree | 20966810 | Detail |
0.122 | pancreatic carcinoma | According to the assumption that genetic variation in carcinogen metabolism furt... | BeFree | 20966810 | Detail |
0.004 | Malignant neoplasm of pancreas | According to the assumption that genetic variation in carcinogen metabolism furt... | BeFree | 20966810 | Detail |
<0.001 | Malignant neoplasm of pancreas | According to the assumption that genetic variation in carcinogen metabolism furt... | BeFree | 20966810 | Detail |
<0.001 | Stage IV Prostate Cancer AJCC v7 | Seven interactions were statistically significant after adjusting for multiple t... | BeFree | 25315963 | Detail |
<0.001 | Stage IV Prostate Cancer AJCC v7 | Seven interactions were statistically significant after adjusting for multiple t... | BeFree | 25315963 | Detail |
<0.001 | Stage IV Prostate Cancer AJCC v7 | Seven interactions were statistically significant after adjusting for multiple t... | BeFree | 25315963 | Detail |
<0.001 | Stage IV Prostate Carcinoma | Seven interactions were statistically significant after adjusting for multiple t... | BeFree | 25315963 | Detail |
<0.001 | Stage IV Prostate Carcinoma | Seven interactions were statistically significant after adjusting for multiple t... | BeFree | 25315963 | Detail |
<0.001 | Stage IV Prostate Carcinoma | Seven interactions were statistically significant after adjusting for multiple t... | BeFree | 25315963 | Detail |
0.005 | prostate carcinoma | A high tertile selenium level in combination with non-wt rs125701 of the OGG1 ge... | BeFree | 21982398 | Detail |
0.045 | Malignant neoplasm of prostate | A high tertile selenium level in combination with non-wt rs125701 of the OGG1 ge... | BeFree | 21982398 | Detail |
0.004 | prostate carcinoma | A high tertile selenium level in combination with non-wt rs125701 of the OGG1 ge... | BeFree | 21982398 | Detail |
0.020 | Malignant neoplasm of prostate | A high tertile selenium level in combination with non-wt rs125701 of the OGG1 ge... | BeFree | 21982398 | Detail |
<0.001 | Secondary malignant neoplasm of lymph node | The SOD2 rs4880 CT + CC genotypes were significantly associated with a high leve... | BeFree | 22517484 | Detail |
0.001 | Secondary malignant neoplasm of lymph node | The SOD2 rs4880 CT + CC genotypes were significantly associated with a high leve... | BeFree | 22517484 | Detail |
<0.001 | Tumor Progression | The current data, based on a large cohort (n = 929) of Chinese patients with gas... | BeFree | 22517484 | Detail |
0.001 | Tumor Progression | The current data, based on a large cohort (n = 929) of Chinese patients with gas... | BeFree | 22517484 | Detail |
0.007 | Diabetes Mellitus, Non-Insulin-Dependent | To evaluate whether the genetic polymorphisms of glutathione S-transferases M1 (... | BeFree | 24685594 | Detail |
<0.001 | Carotid Atherosclerosis | The aim of the present study was to test the association between genetic polymor... | BeFree | 22330623 | Detail |
0.143 | Diabetes Mellitus, Non-Insulin-Dependent | The aim of the present study was to test the association between genetic polymor... | BeFree | 22330623 | Detail |
0.007 | Diabetes Mellitus, Non-Insulin-Dependent | The aim of the present study was to test the association between genetic polymor... | BeFree | 22330623 | Detail |
0.143 | Diabetes Mellitus, Non-Insulin-Dependent | To evaluate whether the genetic polymorphisms of glutathione S-transferases M1 (... | BeFree | 24685594 | Detail |
<0.001 | B-Cell Lymphomas | In an analysis of manganese superoxide dismutase (SOD2 Val16Ala, rs1799725) Ala/... | BeFree | 16543247 | Detail |
0.189 | Cardiovascular Diseases | We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males... | BeFree | 24933031 | Detail |
<0.001 | Cardiovascular Diseases | We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males... | BeFree | 24933031 | Detail |
0.008 | Cardiovascular Diseases | We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males... | BeFree | 24933031 | Detail |
0.027 | Coronary heart disease | We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males... | BeFree | 24933031 | Detail |
0.005 | Coronary heart disease | We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males... | BeFree | 24933031 | Detail |
<0.001 | Cardiovascular Diseases | We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males... | BeFree | 24933031 | Detail |
0.044 | Coronary heart disease | We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males... | BeFree | 24933031 | Detail |
0.125 | Cardiovascular Diseases | We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males... | BeFree | 24933031 | Detail |
0.003 | Coronary heart disease | We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males... | BeFree | 24933031 | Detail |
0.005 | Coronary heart disease | We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males... | BeFree | 24933031 | Detail |
0.010 | Tardive Dyskinesia | Search for these determinants has led to a few consensus associations of CYP2D6 ... | BeFree | 18781856 | Detail |
0.013 | Tardive Dyskinesia | Search for these determinants has led to a few consensus associations of CYP2D6 ... | BeFree | 18781856 | Detail |
0.010 | lingual-facial-buccal dyskinesia | Search for these determinants has led to a few consensus associations of CYP2D6 ... | BeFree | 18781856 | Detail |
0.032 | lingual-facial-buccal dyskinesia | Search for these determinants has led to a few consensus associations of CYP2D6 ... | BeFree | 18781856 | Detail |
0.016 | Tardive Dyskinesia | Search for these determinants has led to a few consensus associations of CYP2D6 ... | BeFree | 18781856 | Detail |
0.013 | lingual-facial-buccal dyskinesia | Search for these determinants has led to a few consensus associations of CYP2D6 ... | BeFree | 18781856 | Detail |
0.019 | lingual-facial-buccal dyskinesia | Search for these determinants has led to a few consensus associations of CYP2D6 ... | BeFree | 18781856 | Detail |
0.006 | lingual-facial-buccal dyskinesia | Search for these determinants has led to a few consensus associations of CYP2D6 ... | BeFree | 18781856 | Detail |
0.006 | Tardive Dyskinesia | Search for these determinants has led to a few consensus associations of CYP2D6 ... | BeFree | 18781856 | Detail |
0.037 | Tardive Dyskinesia | Search for these determinants has led to a few consensus associations of CYP2D6 ... | BeFree | 18781856 | Detail |
0.003 | Carcinoma of lung | A review was conducted of 136 patients treated with radiation therapy for lung c... | BeFree | 22144047 | Detail |
0.022 | Malignant neoplasm of lung | A review was conducted of 136 patients treated with radiation therapy for lung c... | BeFree | 22144047 | Detail |
0.002 | Carcinoma of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.066 | Malignant neoplasm of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.002 | Malignant neoplasm of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.002 | Malignant neoplasm of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.002 | Carcinoma of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.002 | Malignant neoplasm of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.002 | Carcinoma of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.009 | Carcinoma of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.002 | Malignant neoplasm of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.002 | Carcinoma of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.003 | Carcinoma of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.002 | Carcinoma of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.012 | Carcinoma of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.012 | Malignant neoplasm of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.092 | Malignant neoplasm of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.022 | Malignant neoplasm of lung | However, only four of the previously reported associations with polymorphisms in... | BeFree | 18258609 | Detail |
0.001 | Diabetes | (i) to determine the extent of oxidative stress and DNA damage and repair using ... | BeFree | 21338322 | Detail |
0.440 | obesity | Association of the Ala16Val MnSOD gene polymorphism with plasma leptin levels an... | BeFree | 25958349 | Detail |
0.009 | liver carcinoma | No significant associations were observed between three other polymorphisms (MnS... | BeFree | 25894370 | Detail |
0.022 | Malignant neoplasm of lung | Although the majority of evidence supports associations between the SOD2 Ala16Va... | BeFree | 22525041 | Detail |
0.006 | coronary artery disease | Association of C47T polymorphism in SOD2 gene with coronary artery disease: a ca... | BeFree | 22170599 | Detail |
0.123 | Liver Cirrhosis, Alcoholic | Our aim was to determine whether Ala16Val-superoxide dismutase 2 (SOD2), G-463A-... | BeFree | 19731237 | Detail |
<0.001 | Acute coronary syndrome | The aim was to determine (a) Ala-16Val-SOD2 dimorphisms; (b) allelic frequency a... | BeFree | 21062213 | Detail |
0.074 | Malignant neoplasm of breast | We studied the possible association between Ala16Val manganese-dependent superox... | BeFree | 20082851 | Detail |
0.122 | pancreatic carcinoma | Polymorphisms of the inflammatory pathway genes MPO -G463A and SOD2 Ala16Val are... | BeFree | 18205184 | Detail |
0.001 | ovarian carcinoma | Functional variant of manganese superoxide dismutase (SOD2 V16A) polymorphism is... | BeFree | 17646272 | Detail |
0.005 | Non-small cell lung carcinoma | In this case-control study (830 non-small cell lung carcinoma (NSCLC) patients; ... | BeFree | 15331175 | Detail |
<0.001 | Fibrosis, Liver | The aim of the present study was to investigate the influence of MPO G-463A and ... | BeFree | 24882572 | Detail |
<0.001 | lymphoma | Data from two population-based, case-control studies of lymphoma in the UK (700 ... | BeFree | 16956821 | Detail |
0.010 | breast carcinoma | We studied the possible association between Ala16Val manganese-dependent superox... | BeFree | 20082851 | Detail |
0.143 | Diabetes Mellitus, Non-Insulin-Dependent | SOD2 gene Val16Ala polymorphism is associated with macroalbuminuria in Mexican t... | BeFree | 24119114 | Detail |
<0.001 | lymphoma | Data from two population-based, case-control studies of lymphoma in the UK (700 ... | BeFree | 16956821 | Detail |
0.045 | Malignant neoplasm of prostate | Functional variant of manganese superoxide dismutase (SOD2 V16A) polymorphism is... | BeFree | 17646272 | Detail |
0.003 | Coronary Arteriosclerosis | Association of C47T polymorphism in SOD2 gene with coronary artery disease: a ca... | BeFree | 22170599 | Detail |
0.074 | Malignant neoplasm of breast | No association between SOD2 Val16Ala polymorphism and breast cancer susceptibili... | BeFree | 20052533 | Detail |
<0.001 | Malignant neoplasm of pancreas | Polymorphisms of the inflammatory pathway genes MPO -G463A and SOD2 Ala16Val are... | BeFree | 18205184 | Detail |
0.123 | Cardiomyopathy, Dilated | The aim was to determine (a) Ala-16Val-SOD2 dimorphisms; (b) allelic frequency a... | BeFree | 21062213 | Detail |
0.003 | Carcinoma of lung | Association between SOD2 C47T polymorphism and lung cancer susceptibility: a met... | BeFree | 23990443 | Detail |
0.001 | stomach carcinoma | To investigate the association between MnSOD Val(16)Ala polymorphism and risk of... | BeFree | 20233853 | Detail |
<0.001 | migraine with aura | Is SOD2 Ala16Val polymorphism associated with migraine with aura phenotype? | BeFree | 25295643 | Detail |
0.005 | Coronary heart disease | Association of C47T polymorphism in SOD2 gene with coronary artery disease: a ca... | BeFree | 22170599 | Detail |
0.014 | Diabetes Mellitus, Insulin-Dependent | The V16A polymorphism in SOD2 is associated with increased risk of diabetic neph... | BeFree | 19834686 | Detail |
<0.001 | Cardiovascular Diseases | The V16A polymorphism in SOD2 is associated with increased risk of diabetic neph... | BeFree | 19834686 | Detail |
0.010 | breast carcinoma | Our findings suggest that the SOD2 Val16Ala variant is not related to the risk o... | BeFree | 21056286 | Detail |
<0.001 | lymphoma | Data from two population-based, case-control studies of lymphoma in the UK (700 ... | BeFree | 16956821 | Detail |
0.006 | asthma | To investigate the association of the manganese-containing form of SOD (MnSOD) g... | BeFree | 16630148 | Detail |
0.022 | Malignant neoplasm of lung | Association between SOD2 C47T polymorphism and lung cancer susceptibility: a met... | BeFree | 23990443 | Detail |
0.005 | hepatitis C | The aim of the present study was to investigate the influence of MPO G-463A and ... | BeFree | 24882572 | Detail |
<0.001 | epilepsy | The association between the superoxide dismutase 2 (SOD2) Val16Ala polymorphism ... | BeFree | 22119635 | Detail |
0.121 | male infertility | The results indicated that the PON1 Arg192Glu (rs662) and SOD2 Val16Ala (rs4880)... | BeFree | 22206979 | Detail |
0.008 | diabetic retinopathy | A statistically significant association of MnSOD Ala16Val polymorphism with diab... | BeFree | 19628492 | Detail |
0.004 | Malignant neoplasm of stomach | To investigate the association between MnSOD Val(16)Ala polymorphism and risk of... | BeFree | 20233853 | Detail |
0.074 | Malignant neoplasm of breast | Lack of association between MnSOD Val16Ala polymorphism and breast cancer risk: ... | BeFree | 20143154 | Detail |
<0.001 | pancreatic carcinoma | Polymorphisms of the inflammatory pathway genes MPO -G463A and SOD2 Ala16Val are... | BeFree | 18205184 | Detail |
<0.001 | Carcinogenesis | The higher activity Ala variant at SOD2 Ex2+24T>C (V16A), which has been hypo... | BeFree | 17646272 | Detail |
0.123 | obesity | Association of the Ala16Val MnSOD gene polymorphism with plasma leptin levels an... | BeFree | 25958349 | Detail |
0.011 | Malignant neoplasm of ovary | Functional variant of manganese superoxide dismutase (SOD2 V16A) polymorphism is... | BeFree | 17646272 | Detail |
<0.001 | Fibrosis, Liver | The aim of the present study was to investigate the influence of MPO G-463A and ... | BeFree | 24882572 | Detail |
0.074 | Malignant neoplasm of breast | Our findings suggest that the SOD2 Val16Ala variant is not related to the risk o... | BeFree | 21056286 | Detail |
0.010 | breast carcinoma | Lack of association between MnSOD Val16Ala polymorphism and breast cancer risk: ... | BeFree | 20143154 | Detail |
<0.001 | Demyelinating Diseases | We tested an SOD2 variant C47T (Ala16Val) associated with reduced enzymatic acti... | BeFree | 22218650 | Detail |
<0.001 | epilepsy | Our results showed that the SOD2 Val16Ala polymorphism has an impact on the rela... | BeFree | 25372290 | Detail |
<0.001 | Hearing Loss, Mixed Conductive-Sensorineural | SOD2 V16A SNP in the mitochondrial targeting sequence is associated with noise i... | BeFree | 20534900 | Detail |
0.123 | male infertility | The results indicated that the PON1 Arg192Glu (rs662) and SOD2 Val16Ala (rs4880)... | BeFree | 22206979 | Detail |
0.009 | liver carcinoma | Our aim was to determine whether Ala16Val-superoxide dismutase 2 (SOD2), G-463A-... | BeFree | 19731237 | Detail |
0.014 | age related macular degeneration | We found no evidence to support the role of any common SOD2 variations including... | BeFree | 19753309 | Detail |
<0.001 | Non-alcoholic Fatty Liver Disease | The SOD2 C47T polymorphism influences NAFLD fibrosis severity: evidence from cas... | BeFree | 21756849 | Detail |
0.120 | Acute coronary syndrome | The aim was to determine (a) Ala-16Val-SOD2 dimorphisms; (b) allelic frequency a... | BeFree | 21062213 | Detail |
0.045 | Malignant neoplasm of prostate | To examine the association between 2 mitochondrial manganese superoxide dismutas... | BeFree | 19647296 | Detail |
0.121 | Cardiomyopathy, Dilated | The aim was to determine (a) Ala-16Val-SOD2 dimorphisms; (b) allelic frequency a... | BeFree | 21062213 | Detail |
0.005 | prostate carcinoma | To examine the association between 2 mitochondrial manganese superoxide dismutas... | BeFree | 19647296 | Detail |
<0.001 | Malignant neoplasm of skin | We assessed whether the functional V16A polymorphism in the MnSOD gene is associ... | BeFree | 17186424 | Detail |
<0.001 | lymphoma | Data from two population-based, case-control studies of lymphoma in the UK (700 ... | BeFree | 16956821 | Detail |
0.004 | Malignant neoplasm of pancreas | Polymorphisms of the inflammatory pathway genes MPO -G463A and SOD2 Ala16Val are... | BeFree | 18205184 | Detail |
0.128 | Diabetic Nephropathy | The V16A polymorphism in SOD2 is associated with increased risk of diabetic neph... | BeFree | 19834686 | Detail |
0.010 | breast carcinoma | No association between SOD2 Val16Ala polymorphism and breast cancer susceptibili... | BeFree | 20052533 | Detail |
0.005 | prostate carcinoma | Functional variant of manganese superoxide dismutase (SOD2 V16A) polymorphism is... | BeFree | 17646272 | Detail |
0.129 | liver carcinoma | No significant associations were observed between three other polymorphisms (MnS... | BeFree | 25894370 | Detail |
0.131 | diabetes mellitus | (i) to determine the extent of oxidative stress and DNA damage and repair using ... | BeFree | 21338322 | Detail |
0.045 | Malignant neoplasm of prostate | In the present study we investigated the association of a number of polymorphic ... | BeFree | 24610081 | Detail |
0.002 | Carcinoma of lung | We evaluated potential associations between gene variants that result in reduced... | BeFree | 17548672 | Detail |
0.004 | prostate carcinoma | In the present study we investigated the association of a number of polymorphic ... | BeFree | 24610081 | Detail |
0.003 | Carcinoma of lung | We evaluated potential associations between gene variants that result in reduced... | BeFree | 17548672 | Detail |
0.005 | prostate carcinoma | In the present study we investigated the association of a number of polymorphic ... | BeFree | 24610081 | Detail |
0.013 | Malignant neoplasm of prostate | In the present study we investigated the association of a number of polymorphic ... | BeFree | 24610081 | Detail |
0.087 | Malignant neoplasm of prostate | In the present study we investigated the association of a number of polymorphic ... | BeFree | 24610081 | Detail |
0.022 | Malignant neoplasm of lung | We evaluated potential associations between gene variants that result in reduced... | BeFree | 17548672 | Detail |
0.026 | prostate carcinoma | In the present study we investigated the association of a number of polymorphic ... | BeFree | 24610081 | Detail |
0.026 | Malignant neoplasm of lung | We evaluated potential associations between gene variants that result in reduced... | BeFree | 17548672 | Detail |
0.005 | Coronary heart disease | [Association between the rs4880 superoxide dismutase 2 (C>T) gene variant and co... | GAD | 20728955 | Detail |
<0.001 | Septicemia | Evaluating the subgroup of 293 ICU patients with sepsis, a pooled analysis inclu... | BeFree | 25497738 | Detail |
<0.001 | Sepsis | Evaluating the subgroup of 293 ICU patients with sepsis, a pooled analysis inclu... | BeFree | 25497738 | Detail |
<0.001 | Hearing Loss, Mixed Conductive-Sensorineural | The C allele of SOD2 (rs4880) was more frequent in Ménière's disease cases with ... | BeFree | 22877234 | Detail |
0.240 | MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (finding) | NA | CLINVAR | Detail | |
0.074 | Malignant neoplasm of breast | [Our results are consistent with the hypothesis that women with higher SOD2 anti... | GAD | 20309628 | Detail |
0.005 | Diabetic Angiopathies | [Association between the rs4880 superoxide dismutase 2 (C>T) gene variant and co... | GAD | 20728955 | Detail |
<0.001 | Migraine Disorders | We also found a mild correlation between SOD2 rs4880 genotype and the type of ac... | BeFree | 25295643 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000636.4(SOD2):c.47T>C (p.Val16Ala) AND SUPEROXIDE DISMUTASE 2 POLYMORPHISM | ClinVar | Detail |
NM_000636.4(SOD2):c.47T>C (p.Val16Ala) AND Microvascular complications of diabetes, susceptibility t... | ClinVar | Detail |
Six SNPs of five genes (rs1800562 of HFE, rs17868323 and rs11692021 of UGT1A7, rs2279744 of MDM2, rs... | DisGeNET | Detail |
Six SNPs of five genes (rs1800562 of HFE, rs17868323 and rs11692021 of UGT1A7, rs2279744 of MDM2, rs... | DisGeNET | Detail |
Six SNPs of five genes (rs1800562 of HFE, rs17868323 and rs11692021 of UGT1A7, rs2279744 of MDM2, rs... | DisGeNET | Detail |
According to the assumption that genetic variation in carcinogen metabolism further modifies the ris... | DisGeNET | Detail |
According to the assumption that genetic variation in carcinogen metabolism further modifies the ris... | DisGeNET | Detail |
According to the assumption that genetic variation in carcinogen metabolism further modifies the ris... | DisGeNET | Detail |
According to the assumption that genetic variation in carcinogen metabolism further modifies the ris... | DisGeNET | Detail |
Seven interactions were statistically significant after adjusting for multiple testing (FDR Q-value ... | DisGeNET | Detail |
Seven interactions were statistically significant after adjusting for multiple testing (FDR Q-value ... | DisGeNET | Detail |
Seven interactions were statistically significant after adjusting for multiple testing (FDR Q-value ... | DisGeNET | Detail |
Seven interactions were statistically significant after adjusting for multiple testing (FDR Q-value ... | DisGeNET | Detail |
Seven interactions were statistically significant after adjusting for multiple testing (FDR Q-value ... | DisGeNET | Detail |
Seven interactions were statistically significant after adjusting for multiple testing (FDR Q-value ... | DisGeNET | Detail |
A high tertile selenium level in combination with non-wt rs125701 of the OGG1 gene in combination wi... | DisGeNET | Detail |
A high tertile selenium level in combination with non-wt rs125701 of the OGG1 gene in combination wi... | DisGeNET | Detail |
A high tertile selenium level in combination with non-wt rs125701 of the OGG1 gene in combination wi... | DisGeNET | Detail |
A high tertile selenium level in combination with non-wt rs125701 of the OGG1 gene in combination wi... | DisGeNET | Detail |
The SOD2 rs4880 CT + CC genotypes were significantly associated with a high level of lymph node meta... | DisGeNET | Detail |
The SOD2 rs4880 CT + CC genotypes were significantly associated with a high level of lymph node meta... | DisGeNET | Detail |
The current data, based on a large cohort (n = 929) of Chinese patients with gastric cancer, suggest... | DisGeNET | Detail |
The current data, based on a large cohort (n = 929) of Chinese patients with gastric cancer, suggest... | DisGeNET | Detail |
To evaluate whether the genetic polymorphisms of glutathione S-transferases M1 (GSTM1) and T1 (GSTT1... | DisGeNET | Detail |
The aim of the present study was to test the association between genetic polymorphisms with function... | DisGeNET | Detail |
The aim of the present study was to test the association between genetic polymorphisms with function... | DisGeNET | Detail |
The aim of the present study was to test the association between genetic polymorphisms with function... | DisGeNET | Detail |
To evaluate whether the genetic polymorphisms of glutathione S-transferases M1 (GSTM1) and T1 (GSTT1... | DisGeNET | Detail |
In an analysis of manganese superoxide dismutase (SOD2 Val16Ala, rs1799725) Ala/Ala homozygotes, we ... | DisGeNET | Detail |
We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males 66.1%, 59.5 ± 10.0 ... | DisGeNET | Detail |
We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males 66.1%, 59.5 ± 10.0 ... | DisGeNET | Detail |
We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males 66.1%, 59.5 ± 10.0 ... | DisGeNET | Detail |
We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males 66.1%, 59.5 ± 10.0 ... | DisGeNET | Detail |
We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males 66.1%, 59.5 ± 10.0 ... | DisGeNET | Detail |
We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males 66.1%, 59.5 ± 10.0 ... | DisGeNET | Detail |
We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males 66.1%, 59.5 ± 10.0 ... | DisGeNET | Detail |
We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males 66.1%, 59.5 ± 10.0 ... | DisGeNET | Detail |
We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males 66.1%, 59.5 ± 10.0 ... | DisGeNET | Detail |
We enrolled 1977 Japanese type 2 diabetic subjects without history of CVD (males 66.1%, 59.5 ± 10.0 ... | DisGeNET | Detail |
Search for these determinants has led to a few consensus associations of CYP2D6 *10, CYP1A2*1F, DRD2... | DisGeNET | Detail |
Search for these determinants has led to a few consensus associations of CYP2D6 *10, CYP1A2*1F, DRD2... | DisGeNET | Detail |
Search for these determinants has led to a few consensus associations of CYP2D6 *10, CYP1A2*1F, DRD2... | DisGeNET | Detail |
Search for these determinants has led to a few consensus associations of CYP2D6 *10, CYP1A2*1F, DRD2... | DisGeNET | Detail |
Search for these determinants has led to a few consensus associations of CYP2D6 *10, CYP1A2*1F, DRD2... | DisGeNET | Detail |
Search for these determinants has led to a few consensus associations of CYP2D6 *10, CYP1A2*1F, DRD2... | DisGeNET | Detail |
Search for these determinants has led to a few consensus associations of CYP2D6 *10, CYP1A2*1F, DRD2... | DisGeNET | Detail |
Search for these determinants has led to a few consensus associations of CYP2D6 *10, CYP1A2*1F, DRD2... | DisGeNET | Detail |
Search for these determinants has led to a few consensus associations of CYP2D6 *10, CYP1A2*1F, DRD2... | DisGeNET | Detail |
Search for these determinants has led to a few consensus associations of CYP2D6 *10, CYP1A2*1F, DRD2... | DisGeNET | Detail |
A review was conducted of 136 patients treated with radiation therapy for lung cancer between 2001 a... | DisGeNET | Detail |
A review was conducted of 136 patients treated with radiation therapy for lung cancer between 2001 a... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
However, only four of the previously reported associations with polymorphisms in the GSTP1 (Ala14Val... | DisGeNET | Detail |
(i) to determine the extent of oxidative stress and DNA damage and repair using a panel of selected ... | DisGeNET | Detail |
Association of the Ala16Val MnSOD gene polymorphism with plasma leptin levels and oxidative stress b... | DisGeNET | Detail |
No significant associations were observed between three other polymorphisms (MnSOD Ala16Val, CAT-262... | DisGeNET | Detail |
Although the majority of evidence supports associations between the SOD2 Ala16Val SNP and diseases s... | DisGeNET | Detail |
Association of C47T polymorphism in SOD2 gene with coronary artery disease: a case-control study and... | DisGeNET | Detail |
Our aim was to determine whether Ala16Val-superoxide dismutase 2 (SOD2), G-463A-MPO, or T-262C-CAT d... | DisGeNET | Detail |
The aim was to determine (a) Ala-16Val-SOD2 dimorphisms; (b) allelic frequency and phenotype of a co... | DisGeNET | Detail |
We studied the possible association between Ala16Val manganese-dependent superoxide dismutase (MnSOD... | DisGeNET | Detail |
Polymorphisms of the inflammatory pathway genes MPO -G463A and SOD2 Ala16Val are associated with ele... | DisGeNET | Detail |
Functional variant of manganese superoxide dismutase (SOD2 V16A) polymorphism is associated with pro... | DisGeNET | Detail |
In this case-control study (830 non-small cell lung carcinoma (NSCLC) patients; 1119 controls) we ev... | DisGeNET | Detail |
The aim of the present study was to investigate the influence of MPO G-463A and SOD2 Ala16Val polymo... | DisGeNET | Detail |
Data from two population-based, case-control studies of lymphoma in the UK (700 cases and 915 contro... | DisGeNET | Detail |
We studied the possible association between Ala16Val manganese-dependent superoxide dismutase (MnSOD... | DisGeNET | Detail |
SOD2 gene Val16Ala polymorphism is associated with macroalbuminuria in Mexican type 2 diabetes patie... | DisGeNET | Detail |
Data from two population-based, case-control studies of lymphoma in the UK (700 cases and 915 contro... | DisGeNET | Detail |
Functional variant of manganese superoxide dismutase (SOD2 V16A) polymorphism is associated with pro... | DisGeNET | Detail |
Association of C47T polymorphism in SOD2 gene with coronary artery disease: a case-control study and... | DisGeNET | Detail |
No association between SOD2 Val16Ala polymorphism and breast cancer susceptibility: a meta-analysis ... | DisGeNET | Detail |
Polymorphisms of the inflammatory pathway genes MPO -G463A and SOD2 Ala16Val are associated with ele... | DisGeNET | Detail |
The aim was to determine (a) Ala-16Val-SOD2 dimorphisms; (b) allelic frequency and phenotype of a co... | DisGeNET | Detail |
Association between SOD2 C47T polymorphism and lung cancer susceptibility: a meta-analysis. | DisGeNET | Detail |
To investigate the association between MnSOD Val(16)Ala polymorphism and risk of advanced gastric le... | DisGeNET | Detail |
Is SOD2 Ala16Val polymorphism associated with migraine with aura phenotype? | DisGeNET | Detail |
Association of C47T polymorphism in SOD2 gene with coronary artery disease: a case-control study and... | DisGeNET | Detail |
The V16A polymorphism in SOD2 is associated with increased risk of diabetic nephropathy and cardiova... | DisGeNET | Detail |
The V16A polymorphism in SOD2 is associated with increased risk of diabetic nephropathy and cardiova... | DisGeNET | Detail |
Our findings suggest that the SOD2 Val16Ala variant is not related to the risk of breast cancer in K... | DisGeNET | Detail |
Data from two population-based, case-control studies of lymphoma in the UK (700 cases and 915 contro... | DisGeNET | Detail |
To investigate the association of the manganese-containing form of SOD (MnSOD) gene at amino acid po... | DisGeNET | Detail |
Association between SOD2 C47T polymorphism and lung cancer susceptibility: a meta-analysis. | DisGeNET | Detail |
The aim of the present study was to investigate the influence of MPO G-463A and SOD2 Ala16Val polymo... | DisGeNET | Detail |
The association between the superoxide dismutase 2 (SOD2) Val16Ala polymorphism and the serum aminot... | DisGeNET | Detail |
The results indicated that the PON1 Arg192Glu (rs662) and SOD2 Val16Ala (rs4880) variant genotypes w... | DisGeNET | Detail |
A statistically significant association of MnSOD Ala16Val polymorphism with diabetic retinopathy was... | DisGeNET | Detail |
To investigate the association between MnSOD Val(16)Ala polymorphism and risk of advanced gastric le... | DisGeNET | Detail |
Lack of association between MnSOD Val16Ala polymorphism and breast cancer risk: a meta-analysis invo... | DisGeNET | Detail |
Polymorphisms of the inflammatory pathway genes MPO -G463A and SOD2 Ala16Val are associated with ele... | DisGeNET | Detail |
The higher activity Ala variant at SOD2 Ex2+24T>C (V16A), which has been hypothesized to suppress... | DisGeNET | Detail |
Association of the Ala16Val MnSOD gene polymorphism with plasma leptin levels and oxidative stress b... | DisGeNET | Detail |
Functional variant of manganese superoxide dismutase (SOD2 V16A) polymorphism is associated with pro... | DisGeNET | Detail |
The aim of the present study was to investigate the influence of MPO G-463A and SOD2 Ala16Val polymo... | DisGeNET | Detail |
Our findings suggest that the SOD2 Val16Ala variant is not related to the risk of breast cancer in K... | DisGeNET | Detail |
Lack of association between MnSOD Val16Ala polymorphism and breast cancer risk: a meta-analysis invo... | DisGeNET | Detail |
We tested an SOD2 variant C47T (Ala16Val) associated with reduced enzymatic activity as a potential ... | DisGeNET | Detail |
Our results showed that the SOD2 Val16Ala polymorphism has an impact on the relationship between VPA... | DisGeNET | Detail |
SOD2 V16A SNP in the mitochondrial targeting sequence is associated with noise induced hearing loss ... | DisGeNET | Detail |
The results indicated that the PON1 Arg192Glu (rs662) and SOD2 Val16Ala (rs4880) variant genotypes w... | DisGeNET | Detail |
Our aim was to determine whether Ala16Val-superoxide dismutase 2 (SOD2), G-463A-MPO, or T-262C-CAT d... | DisGeNET | Detail |
We found no evidence to support the role of any common SOD2 variations including the V16A variant in... | DisGeNET | Detail |
The SOD2 C47T polymorphism influences NAFLD fibrosis severity: evidence from case-control and intra-... | DisGeNET | Detail |
The aim was to determine (a) Ala-16Val-SOD2 dimorphisms; (b) allelic frequency and phenotype of a co... | DisGeNET | Detail |
To examine the association between 2 mitochondrial manganese superoxide dismutase (MnSOD) genetic po... | DisGeNET | Detail |
The aim was to determine (a) Ala-16Val-SOD2 dimorphisms; (b) allelic frequency and phenotype of a co... | DisGeNET | Detail |
To examine the association between 2 mitochondrial manganese superoxide dismutase (MnSOD) genetic po... | DisGeNET | Detail |
We assessed whether the functional V16A polymorphism in the MnSOD gene is associated with skin cance... | DisGeNET | Detail |
Data from two population-based, case-control studies of lymphoma in the UK (700 cases and 915 contro... | DisGeNET | Detail |
Polymorphisms of the inflammatory pathway genes MPO -G463A and SOD2 Ala16Val are associated with ele... | DisGeNET | Detail |
The V16A polymorphism in SOD2 is associated with increased risk of diabetic nephropathy and cardiova... | DisGeNET | Detail |
No association between SOD2 Val16Ala polymorphism and breast cancer susceptibility: a meta-analysis ... | DisGeNET | Detail |
Functional variant of manganese superoxide dismutase (SOD2 V16A) polymorphism is associated with pro... | DisGeNET | Detail |
No significant associations were observed between three other polymorphisms (MnSOD Ala16Val, CAT-262... | DisGeNET | Detail |
(i) to determine the extent of oxidative stress and DNA damage and repair using a panel of selected ... | DisGeNET | Detail |
In the present study we investigated the association of a number of polymorphic changes in antioxida... | DisGeNET | Detail |
We evaluated potential associations between gene variants that result in reduced neutralization of r... | DisGeNET | Detail |
In the present study we investigated the association of a number of polymorphic changes in antioxida... | DisGeNET | Detail |
We evaluated potential associations between gene variants that result in reduced neutralization of r... | DisGeNET | Detail |
In the present study we investigated the association of a number of polymorphic changes in antioxida... | DisGeNET | Detail |
In the present study we investigated the association of a number of polymorphic changes in antioxida... | DisGeNET | Detail |
In the present study we investigated the association of a number of polymorphic changes in antioxida... | DisGeNET | Detail |
We evaluated potential associations between gene variants that result in reduced neutralization of r... | DisGeNET | Detail |
In the present study we investigated the association of a number of polymorphic changes in antioxida... | DisGeNET | Detail |
We evaluated potential associations between gene variants that result in reduced neutralization of r... | DisGeNET | Detail |
[Association between the rs4880 superoxide dismutase 2 (C>T) gene variant and coronary heart disease... | DisGeNET | Detail |
Evaluating the subgroup of 293 ICU patients with sepsis, a pooled analysis including two genetic var... | DisGeNET | Detail |
Evaluating the subgroup of 293 ICU patients with sepsis, a pooled analysis including two genetic var... | DisGeNET | Detail |
The C allele of SOD2 (rs4880) was more frequent in Ménière's disease cases with a hearing level over... | DisGeNET | Detail |
NA | DisGeNET | Detail |
[Our results are consistent with the hypothesis that women with higher SOD2 antioxidant activity may... | DisGeNET | Detail |
[Association between the rs4880 superoxide dismutase 2 (C>T) gene variant and coronary heart disease... | DisGeNET | Detail |
We also found a mild correlation between SOD2 rs4880 genotype and the type of acute migraine treatme... | DisGeNET | Detail |
Overlapped Transcript Coordinates
Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
---|
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs4880 dbSNP
- Genome
- hg19
- Position
- chr6:160,113,872-160,113,872
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- G
- Filtering Status (HGVD)
- PASS
- # of samples (HGVD)
- 1140
- Mean of sample read depth (HGVD)
- 64.84
- Standard deviation of sample read depth (HGVD)
- 28.62
- Number of reference allele (HGVD)
- 2028
- Number of alternative allele (HGVD)
- 252
- Allele Frequency (HGVD)
- 0.11052631578947368
- Gene Symbol (HGVD)
- SOD2
- ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- PASS
- Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- rs4880
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.1223
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 2049
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
- East Asian Chromosome Counts (ExAC)
- 7262
- East Asian Allele Counts (ExAC)
- 1159
- East Asian Heterozygous Counts (ExAC)
- 1003
- East Asian Homozygous Counts (ExAC)
- 78
- East Asian Allele Frequency (ExAC)
- 0.15959790691269624
- Chromosome Counts in All Race (ExAC)
- 110890
- Allele Counts in All Race (ExAC)
- 55710
- Heterozygous Counts in All Race (ExAC)
- 28130
- Homozygous Counts in All Race (ExAC)
- 13790
- Allele Frequency in All Race (ExAC)
- 0.5023897556136712
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