rs2474619
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2474619(A;A) |
Make rs2474619(A;C) |
Make rs2474619(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 90170316 |
Gene | BACH2 |
is a | snp |
is | mentioned by |
dbSNP | rs2474619 |
dbSNP (classic) | rs2474619 |
ClinGen | rs2474619 |
ebi | rs2474619 |
HLI | rs2474619 |
Exac | rs2474619 |
Gnomad | rs2474619 |
Varsome | rs2474619 |
LitVar | rs2474619 |
Map | rs2474619 |
PheGenI | rs2474619 |
Biobank | rs2474619 |
1000 genomes | rs2474619 |
hgdp | rs2474619 |
ensembl | rs2474619 |
geneview | rs2474619 |
scholar | rs2474619 |
rs2474619 | |
pharmgkb | rs2474619 |
gwascentral | rs2474619 |
openSNP | rs2474619 |
23andMe | rs2474619 |
SNPshot | rs2474619 |
SNPdbe | rs2474619 |
MSV3d | rs2474619 |
GWAS Ctlg | rs2474619 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 24346624] Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association study
GWAS snp | |
---|---|
PMID | [PMID 24999842![]() |
Trait | Celiac disease |
Title | Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus. |
Risk Allele | |
P-val | 2E-8 |
Odds Ratio | 1.28 [1.18-1.41] |
[PMID 25873652] No association between Bach2 gene polymorphisms with Vogt-Koyanagi-Harada syndrome (VKH) and Behcet's disease (BD) in a Chinese Han population