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rs9936833

From SNPedia

Orientationplus
Stabilizedplus
Make rs9936833(C;C)
Make rs9936833(C;T)
Make rs9936833(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position86369512
is asnp
is mentioned by
dbSNPrs9936833
ebirs9936833
HLIrs9936833
Exacrs9936833
Varsomers9936833
Maprs9936833
PheGenIrs9936833
hapmaprs9936833
1000 genomesrs9936833
hgdprs9936833
ensemblrs9936833
gopubmedrs9936833
geneviewrs9936833
scholarrs9936833
googlers9936833
pharmgkbrs9936833
gwascentralrs9936833
openSNPrs9936833
23andMers9936833
23andMe allrs9936833
SNP Nexus

SNPshotrs9936833
SNPdbers9936833
MSV3drs9936833
GWAS Ctlgrs9936833
GMAF0.32
Max Magnitude
? (C;C) (C;T) (T;T) 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.


[PMID 25164089OA-icon.png] The OSR1 rs12329305 Polymorphism Contributes to the Development of Congenital Malformations in Cases of Stillborn/Neonatal Death