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rs1531228

From SNPedia

Orientationplus
Stabilizedplus
Make rs1531228(C;C)
Make rs1531228(C;T)
Make rs1531228(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position13476447
is asnp
is mentioned by
dbSNPrs1531228
ebirs1531228
HLIrs1531228
Exacrs1531228
Varsomers1531228
Maprs1531228
PheGenIrs1531228
hapmaprs1531228
1000 genomesrs1531228
hgdprs1531228
ensemblrs1531228
gopubmedrs1531228
geneviewrs1531228
scholarrs1531228
googlers1531228
pharmgkbrs1531228
gwascentralrs1531228
openSNPrs1531228
23andMers1531228
23andMe allrs1531228
SNP Nexus

SNPshotrs1531228
SNPdbers1531228
MSV3drs1531228
GWAS Ctlgrs1531228
GMAF0.1423
Max Magnitude
? (C;C) (C;T) (T;T) 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 9E-6
Odds Ratio .20 [0.10-0.30] unit increase