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rs3757247

From SNPedia

Orientationminus
Stabilizedminus
Make rs3757247(A;A)
Make rs3757247(A;G)
Make rs3757247(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position90247744
GeneBACH2
is asnp
is mentioned by
dbSNPrs3757247
ebirs3757247
HLIrs3757247
Exacrs3757247
Varsomers3757247
Maprs3757247
PheGenIrs3757247
hapmaprs3757247
1000 genomesrs3757247
hgdprs3757247
ensemblrs3757247
gopubmedrs3757247
geneviewrs3757247
scholarrs3757247
googlers3757247
pharmgkbrs3757247
gwascentralrs3757247
openSNPrs3757247
23andMers3757247
23andMe allrs3757247
SNP Nexus

SNPshotrs3757247
SNPdbers3757247
MSV3drs3757247
GWAS Ctlgrs3757247
GMAF0.4077
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18840781OA-icon.png]
Trait Type 1 diabetes
Title Follow up analysis of genome-wide association data identifies novel loci for type 1 diabetes
Risk Allele A
P-val 9.9999999999999995E-7
Odds Ratio 1.13 [1.08-1.19]



GWAS snp
PMID [PMID 22561518OA-icon.png]
Trait
Title Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.
Risk Allele A
P-val 3E-8
Odds Ratio 1.2000 None


GET Evidence
rs3757247
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.40625
summary



[PMID 25873652] No association between Bach2 gene polymorphisms with Vogt-Koyanagi-Harada syndrome (VKH) and Behcet's disease (BD) in a Chinese Han population