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rs1912785

From SNPedia

Orientationplus
Stabilizedplus
Make rs1912785(A;A)
Make rs1912785(A;G)
Make rs1912785(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position146684384
is asnp
is mentioned by
dbSNPrs1912785
ebirs1912785
HLIrs1912785
Exacrs1912785
Varsomers1912785
Maprs1912785
PheGenIrs1912785
hapmaprs1912785
1000 genomesrs1912785
hgdprs1912785
ensemblrs1912785
gopubmedrs1912785
geneviewrs1912785
scholarrs1912785
googlers1912785
pharmgkbrs1912785
gwascentralrs1912785
openSNPrs1912785
23andMers1912785
23andMe allrs1912785
SNP Nexus

SNPshotrs1912785
SNPdbers1912785
MSV3drs1912785
GWAS Ctlgrs1912785
GMAF0.4669
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22961001OA-icon.png]
Trait Barrett's esophagus
Title Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.
Risk Allele
P-val 8E-6
Odds Ratio .15 [0.091-0.209] unit decrease