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rs12901001

From SNPedia

Orientationplus
Stabilizedplus
Make rs12901001(A;A)
Make rs12901001(A;G)
Make rs12901001(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position86316245
GeneAGBL1, OR7E157P
is asnp
is mentioned by
dbSNPrs12901001
ebirs12901001
HLIrs12901001
Exacrs12901001
Varsomers12901001
Maprs12901001
PheGenIrs12901001
hapmaprs12901001
1000 genomesrs12901001
hgdprs12901001
ensemblrs12901001
gopubmedrs12901001
geneviewrs12901001
scholarrs12901001
googlers12901001
pharmgkbrs12901001
gwascentralrs12901001
openSNPrs12901001
23andMers12901001
23andMe allrs12901001
SNP Nexus

SNPshotrs12901001
SNPdbers12901001
MSV3drs12901001
GWAS Ctlgrs12901001
GMAF0.461
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 6E-6
Odds Ratio .15 [0.091-0.209] unit increase