Rs9811792

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Orientationplus
is asnp
is mentioned by
dbSNPrs9811792
PheGenIrs9811792
nextbiors9811792
hapmaprs9811792
1000 genomesrs9811792
hgdprs9811792
ensemblrs9811792
gopubmedrs9811792
geneviewrs9811792
scholarrs9811792
googlers9811792
pharmgkbrs9811792
gwascentralrs9811792
openSNPrs9811792
23andMers9811792
23andMe allrs9811792
SNP Nexus

SNPshotrs9811792
SNPdbers9811792
MSV3drs9811792
Chromosome3
Orientationplus
GMAF0.4601
Position159696998
ReferenceGRCh37 37.1/131
Max Magnitude
Make rs9811792(C;C)
Make rs9811792(C;T)
Make rs9811792(T;T)
? (C;C) (C;T) (T;T) 28
OMIM612008
DescCELIAC DISEASE, SUSCEPTIBILITY TO, 10; CELIAC10
Variant
Relatedalso


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[PMID 18311140OA-icon.png] Newly identified genetic risk variants for celiac disease related to the immune response.


[PMID 19073967OA-icon.png] Shared and distinct genetic variants in type 1 diabetes and celiac disease.