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rs1906493

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1906493(A;A)
Make rs1906493(A;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position126080638
is asnp
is mentioned by
dbSNPrs1906493
ebirs1906493
HLIrs1906493
Exacrs1906493
Varsomers1906493
Maprs1906493
PheGenIrs1906493
hapmaprs1906493
1000 genomesrs1906493
hgdprs1906493
ensemblrs1906493
gopubmedrs1906493
geneviewrs1906493
scholarrs1906493
googlers1906493
pharmgkbrs1906493
gwascentralrs1906493
openSNPrs1906493
23andMers1906493
23andMe allrs1906493
SNP Nexus

SNPshotrs1906493
SNPdbers1906493
MSV3drs1906493
GWAS Ctlgrs1906493
GMAF0.1111
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22412388OA-icon.png]
Trait
Title A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.
Risk Allele A
P-val 0.000003
Odds Ratio 1.1900 None