chr19:41860296:A>G Detail (hg19) (TGFB1, B9D2, TMEM91)

Information

Genome

Assembly Position
hg19 chr19:41,860,296-41,860,296
hg38 chr19:41,354,391-41,354,391 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq
Ensemble ENST00000539627.5:c.-30+3189A>G
ENST00000604123.5:c.142+76A>G
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.493
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance Benign
Review star
Show details
Links
Type Database ID Link
Gene MIM 618294 OMIM
HGNC 32393 HGNC
Ensembl ENSG00000142046 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv62133915 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Benign 2024-01-31 criteria provided, single submitter Familial aplasia of the vermis,Meckel-Gruber syndrome germline Detail
Benign 2024-01-31 criteria provided, single submitter Familial aplasia of the vermis,Meckel-Gruber syndrome germline Detail
Benign 2020-06-30 criteria provided, single submitter not provided germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 aortic aneurysm In this study of the Chinese population, homozygosity of TGFB1 rs1800469-T and A... BeFree 26027897 Detail
0.001 aortic aneurysm In this study of the Chinese population, homozygosity of TGFB1 rs1800469-T and A... BeFree 26027897 Detail
<0.001 migraine with aura Among active migraine with aura, the odds ratios (95% confidence intervals) were... BeFree 19559392 Detail
<0.001 migraine with aura Among active migraine with aura, the odds ratios (95% confidence intervals) were... BeFree 19559392 Detail
<0.001 Common Migraine Among active migraine with aura, the odds ratios (95% confidence intervals) were... BeFree 19559392 Detail
<0.001 migraine with aura Among active migraine with aura, the odds ratios (95% confidence intervals) were... BeFree 19559392 Detail
0.003 Migraine Disorders Regarding any history of migraine, the multivariable-adjusted odds ratios (95% c... BeFree 19559392 Detail
0.123 Migraine Disorders Regarding any history of migraine, the multivariable-adjusted odds ratios (95% c... BeFree 19559392 Detail
0.009 Common Migraine Among active migraine with aura, the odds ratios (95% confidence intervals) were... BeFree 19559392 Detail
<0.001 migraine with aura Among active migraine with aura, the odds ratios (95% confidence intervals) were... BeFree 19559392 Detail
0.139 Migraine Disorders Regarding any history of migraine, the multivariable-adjusted odds ratios (95% c... BeFree 19559392 Detail
<0.001 Common Migraine Among active migraine with aura, the odds ratios (95% confidence intervals) were... BeFree 19559392 Detail
<0.001 migraine with aura Among active migraine with aura, the odds ratios (95% confidence intervals) were... BeFree 19559392 Detail
<0.001 Common Migraine Among active migraine with aura, the odds ratios (95% confidence intervals) were... BeFree 19559392 Detail
<0.001 Common Migraine Among active migraine with aura, the odds ratios (95% confidence intervals) were... BeFree 19559392 Detail
<0.001 Thickening of pleura The TIMP2 rs2277698 SNP and a haplotype consisting of the TGFB1 rs1800469 and rs... BeFree 24142982 Detail
<0.001 Ischemic stroke In the non-hypertensive group, CCL11 rs3744508, LTC4S rs730012, FCER1B rs569108,... BeFree 22769019 Detail
0.150 colorectal cancer Large-scale genetic study in East Asians identifies six new loci associated with... GWASCAT 24836286 Detail
<0.001 Thickening of pleura The TIMP2 rs2277698 SNP and a haplotype consisting of the TGFB1 rs1800469 and rs... BeFree 24142982 Detail
0.126 congenital heart defects To evaluate the impact of transforming growth factor-β1 (TGFβ1), TGFβ receptor I... BeFree 24443223 Detail
0.002 Malignant tumor of colon Both TGFβ1 rs1800469 and rs4803455 were associated with colon cancer [odds ratio... BeFree 21068203 Detail
<0.001 Ischemic Cerebrovascular Accident In the non-hypertensive group, CCL11 rs3744508, LTC4S rs730012, FCER1B rs569108,... BeFree 22769019 Detail
0.006 colon carcinoma Both TGFβ1 rs1800469 and rs4803455 were associated with colon cancer [odds ratio... BeFree 21068203 Detail
0.120 colorectal cancer Large-scale genetic study in East Asians identifies six new loci associated with... GWASCAT 24836286 Detail
<0.001 Thickening of pleura The TIMP2 rs2277698 SNP and a haplotype consisting of the TGFB1 rs1800469 and rs... BeFree 24142982 Detail
0.123 Migraine Disorders [Variants in TNF, CCR2, TGFB1, NOS3, and IL9 were found to be associated with mi... GAD 19559392 Detail
0.019 breast carcinoma Multivariate logistic regression found SNPs in genes important for T helper type... BeFree 23996684 Detail
<0.001 Malignant neoplasm of breast Multivariate logistic regression found SNPs in genes important for T helper type... BeFree 23996684 Detail
<0.001 breast carcinoma Multivariate logistic regression found SNPs in genes important for T helper type... BeFree 23996684 Detail
0.090 Malignant neoplasm of breast Multivariate logistic regression found SNPs in genes important for T helper type... BeFree 23996684 Detail
0.005 Malignant neoplasm of breast Multivariate logistic regression found SNPs in genes important for T helper type... BeFree 23996684 Detail
<0.001 breast carcinoma Multivariate logistic regression found SNPs in genes important for T helper type... BeFree 23996684 Detail
<0.001 Malignant neoplasm of breast Multivariate logistic regression found SNPs in genes important for T helper type... BeFree 23996684 Detail
<0.001 breast carcinoma Multivariate logistic regression found SNPs in genes important for T helper type... BeFree 23996684 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000660.6(TGFB1):c.-1347T>C AND multiple conditions ClinVar Detail
NM_000660.6(TGFB1):c.-1347T>C AND multiple conditions ClinVar Detail
NM_000660.6(TGFB1):c.-1347T>C AND not provided ClinVar Detail
In this study of the Chinese population, homozygosity of TGFB1 rs1800469-T and AGTR1 rs12695895-T mi... DisGeNET Detail
In this study of the Chinese population, homozygosity of TGFB1 rs1800469-T and AGTR1 rs12695895-T mi... DisGeNET Detail
Among active migraine with aura, the odds ratios (95% confidence intervals) were 1.35 (1.0 to 1.81) ... DisGeNET Detail
Among active migraine with aura, the odds ratios (95% confidence intervals) were 1.35 (1.0 to 1.81) ... DisGeNET Detail
Among active migraine with aura, the odds ratios (95% confidence intervals) were 1.35 (1.0 to 1.81) ... DisGeNET Detail
Among active migraine with aura, the odds ratios (95% confidence intervals) were 1.35 (1.0 to 1.81) ... DisGeNET Detail
Regarding any history of migraine, the multivariable-adjusted odds ratios (95% confidence intervals)... DisGeNET Detail
Regarding any history of migraine, the multivariable-adjusted odds ratios (95% confidence intervals)... DisGeNET Detail
Among active migraine with aura, the odds ratios (95% confidence intervals) were 1.35 (1.0 to 1.81) ... DisGeNET Detail
Among active migraine with aura, the odds ratios (95% confidence intervals) were 1.35 (1.0 to 1.81) ... DisGeNET Detail
Regarding any history of migraine, the multivariable-adjusted odds ratios (95% confidence intervals)... DisGeNET Detail
Among active migraine with aura, the odds ratios (95% confidence intervals) were 1.35 (1.0 to 1.81) ... DisGeNET Detail
Among active migraine with aura, the odds ratios (95% confidence intervals) were 1.35 (1.0 to 1.81) ... DisGeNET Detail
Among active migraine with aura, the odds ratios (95% confidence intervals) were 1.35 (1.0 to 1.81) ... DisGeNET Detail
Among active migraine with aura, the odds ratios (95% confidence intervals) were 1.35 (1.0 to 1.81) ... DisGeNET Detail
The TIMP2 rs2277698 SNP and a haplotype consisting of the TGFB1 rs1800469 and rs1800470 SNPs were as... DisGeNET Detail
In the non-hypertensive group, CCL11 rs3744508, LTC4S rs730012, FCER1B rs569108, TGFB1 rs1800469, LT... DisGeNET Detail
Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer r... DisGeNET Detail
The TIMP2 rs2277698 SNP and a haplotype consisting of the TGFB1 rs1800469 and rs1800470 SNPs were as... DisGeNET Detail
To evaluate the impact of transforming growth factor-β1 (TGFβ1), TGFβ receptor II (TGFβR2) and vascu... DisGeNET Detail
Both TGFβ1 rs1800469 and rs4803455 were associated with colon cancer [odds ratio (OR) = 0.65 and 1.4... DisGeNET Detail
In the non-hypertensive group, CCL11 rs3744508, LTC4S rs730012, FCER1B rs569108, TGFB1 rs1800469, LT... DisGeNET Detail
Both TGFβ1 rs1800469 and rs4803455 were associated with colon cancer [odds ratio (OR) = 0.65 and 1.4... DisGeNET Detail
Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer r... DisGeNET Detail
The TIMP2 rs2277698 SNP and a haplotype consisting of the TGFB1 rs1800469 and rs1800470 SNPs were as... DisGeNET Detail
[Variants in TNF, CCR2, TGFB1, NOS3, and IL9 were found to be associated with migraine but did not r... DisGeNET Detail
Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... DisGeNET Detail
Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... DisGeNET Detail
Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... DisGeNET Detail
Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... DisGeNET Detail
Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... DisGeNET Detail
Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... DisGeNET Detail
Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... DisGeNET Detail
Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs1800469 dbSNP
Genome
hg19
Position
chr19:41,860,296-41,860,296
Variant Type
snv
Reference Allele
A
Alternative Allele
G
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))
rs1800469
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.4931
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
8262
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16754
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