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rs2474619

From SNPedia

Orientationplus
Stabilizedplus
Make rs2474619(A;A)
Make rs2474619(A;C)
Make rs2474619(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position90170316
GeneBACH2
is asnp
is mentioned by
dbSNPrs2474619
ebirs2474619
HLIrs2474619
Exacrs2474619
Varsomers2474619
Maprs2474619
PheGenIrs2474619
hapmaprs2474619
1000 genomesrs2474619
hgdprs2474619
ensemblrs2474619
gopubmedrs2474619
geneviewrs2474619
scholarrs2474619
googlers2474619
pharmgkbrs2474619
gwascentralrs2474619
openSNPrs2474619
23andMers2474619
23andMe allrs2474619
SNP Nexus

SNPshotrs2474619
SNPdbers2474619
MSV3drs2474619
GWAS Ctlgrs2474619
Max Magnitude
? (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 24999842OA-icon.png]
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