rs1531228

Orientation

plus

Stabilized

plus

Make rs1531228(C;C)

Make rs1531228(C;T)

Make rs1531228(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

13476447

is a	snp
is	mentioned by
dbSNP	rs1531228
dbSNP (classic)	rs1531228
ClinGen	rs1531228
ebi	rs1531228
HLI	rs1531228
Exac	rs1531228
Gnomad	rs1531228
Varsome	rs1531228
LitVar	rs1531228
Map	rs1531228
PheGenI	rs1531228
Biobank	rs1531228
1000 genomes	rs1531228
hgdp	rs1531228
ensembl	rs1531228
geneview	rs1531228
scholar	rs1531228
google	rs1531228
pharmgkb	rs1531228
gwascentral	rs1531228
openSNP	rs1531228
23andMe	rs1531228
SNPshot	rs1531228
SNPdbe	rs1531228
MSV3d	rs1531228
GWAS Ctlg	rs1531228

GMAF

0.1423

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 22961001]
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