chr4:123377980:A>C Detail (hg19)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr4:123,377,980-123,377,980 |
hg38 | chr4:122,456,825-122,456,825 View the variant detail on this assembly version. |
HGVS
[No Data.]
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.335 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:[No Data.] |
Prediction
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
<0.001 | Addison's disease due to autoimmunity | The association of AAD with IL2 and IL2RA polymorphisms (rs6822844, rs2069762, r... | BeFree | 25347332 | Detail |
<0.001 | Autoimmune Primary Adrenal Insufficiency | The association of AAD with IL2 and IL2RA polymorphisms (rs6822844, rs2069762, r... | BeFree | 25347332 | Detail |
0.002 | prostate carcinoma | We genotyped six variants previously associated with autoimmune disease (namely ... | BeFree | 20184734 | Detail |
0.007 | Malignant neoplasm of prostate | We genotyped six variants previously associated with autoimmune disease (namely ... | BeFree | 20184734 | Detail |
0.017 | Autoimmune Diseases | We genotyped six variants previously associated with autoimmune disease (namely ... | BeFree | 20184734 | Detail |
0.002 | measles | Similarly, two previously reported promoter IL10 and IL2 polymorphisms (rs180089... | BeFree | 21875636 | Detail |
<0.001 | measles | Similarly, two previously reported promoter IL10 and IL2 polymorphisms (rs180089... | BeFree | 21875636 | Detail |
<0.001 | Helicobacter pylori infection | Borderline significant associations were seen between IL2-330G (rs2069762) (OR 1... | BeFree | 21649724 | Detail |
0.001 | Helicobacter pylori infection | Borderline significant associations were seen between IL2-330G (rs2069762) (OR 1... | BeFree | 21649724 | Detail |
0.027 | Diabetes Mellitus, Insulin-Dependent | [Eleven of 52 non-MHC T1D loci showed evidence of association with at least one ... | GAD | 21829393 | Detail |
0.030 | multiple sclerosis | We undertook this study to investigate the potential role of polymorphisms rs313... | BeFree | 19523143 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
The association of AAD with IL2 and IL2RA polymorphisms (rs6822844, rs2069762, rs3136534, rs11594656... | DisGeNET | Detail |
The association of AAD with IL2 and IL2RA polymorphisms (rs6822844, rs2069762, rs3136534, rs11594656... | DisGeNET | Detail |
We genotyped six variants previously associated with autoimmune disease (namely rs13151961, rs131197... | DisGeNET | Detail |
We genotyped six variants previously associated with autoimmune disease (namely rs13151961, rs131197... | DisGeNET | Detail |
We genotyped six variants previously associated with autoimmune disease (namely rs13151961, rs131197... | DisGeNET | Detail |
Similarly, two previously reported promoter IL10 and IL2 polymorphisms (rs1800890 and rs2069762) dem... | DisGeNET | Detail |
Similarly, two previously reported promoter IL10 and IL2 polymorphisms (rs1800890 and rs2069762) dem... | DisGeNET | Detail |
Borderline significant associations were seen between IL2-330G (rs2069762) (OR 1.45, 95% CI 0.95, 2.... | DisGeNET | Detail |
Borderline significant associations were seen between IL2-330G (rs2069762) (OR 1.45, 95% CI 0.95, 2.... | DisGeNET | Detail |
[Eleven of 52 non-MHC T1D loci showed evidence of association with at least one autoantibody at a fa... | DisGeNET | Detail |
We undertook this study to investigate the potential role of polymorphisms rs3136534, rs6822844 and ... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs2069762 dbSNP
- Genome
- hg19
- Position
- chr4:123,377,980-123,377,980
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- C
- 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))
- rs2069762
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.3345
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 5607
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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