Have questions? Visit https://www.reddit.com/r/SNPedia

rs9811792

From SNPedia

Orientationplus
Stabilizedplus
Make rs9811792(C;C)
Make rs9811792(C;T)
Make rs9811792(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position159979210
GeneIL12A-AS1
is asnp
is mentioned by
dbSNPrs9811792
dbSNP (classic)rs9811792
ClinGenrs9811792
ebirs9811792
HLIrs9811792
Exacrs9811792
Gnomadrs9811792
Varsomers9811792
LitVarrs9811792
Maprs9811792
PheGenIrs9811792
Biobankrs9811792
1000 genomesrs9811792
hgdprs9811792
ensemblrs9811792
geneviewrs9811792
scholarrs9811792
googlers9811792
pharmgkbrs9811792
gwascentralrs9811792
openSNPrs9811792
23andMers9811792
SNPshotrs9811792
SNPdbers9811792
MSV3drs9811792
GWAS Ctlgrs9811792
GMAF0.4601
Max Magnitude0
? (C;C) (C;T) (T;T) 28


OMIM612008
DescCELIAC DISEASE, SUSCEPTIBILITY TO, 10; CELIAC10
Variant
Relatedalso


[PMID 19693089] Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort


[PMID 22087237OA-icon.png] Improving the estimation of celiac disease sibling risk by non-HLA genes


[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.