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rs9257809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0
Make rs9257809(A;G)
Make rs9257809(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29388554
is asnp
is mentioned by
dbSNPrs9257809
ebirs9257809
HLIrs9257809
Exacrs9257809
Varsomers9257809
Maprs9257809
PheGenIrs9257809
hapmaprs9257809
1000 genomesrs9257809
hgdprs9257809
ensemblrs9257809
gopubmedrs9257809
geneviewrs9257809
scholarrs9257809
googlers9257809
pharmgkbrs9257809
gwascentralrs9257809
openSNPrs9257809
23andMers9257809
23andMe allrs9257809
SNP Nexus

SNPshotrs9257809
SNPdbers9257809
MSV3drs9257809
GWAS Ctlgrs9257809
GMAF0.04132
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 22961001OA-icon.png] Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus


[PMID 23504527] Barrett associated MHC and FOXF1 variants also increase esophageal carcinoma risk.