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rs12928822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs12928822(C;T)
Make rs12928822(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position11310036
is asnp
is mentioned by
dbSNPrs12928822
ebirs12928822
HLIrs12928822
Exacrs12928822
Varsomers12928822
Maprs12928822
PheGenIrs12928822
hapmaprs12928822
1000 genomesrs12928822
hgdprs12928822
ensemblrs12928822
gopubmedrs12928822
geneviewrs12928822
scholarrs12928822
googlers12928822
pharmgkbrs12928822
gwascentralrs12928822
openSNPrs12928822
23andMers12928822
23andMe allrs12928822
SNP Nexus

SNPshotrs12928822
SNPdbers12928822
MSV3drs12928822
GWAS Ctlgrs12928822
GMAF0.09091
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele
P-val 3E-8
Odds Ratio 1.16 [1.10-1.22]

[PMID 19557189OA-icon.png] Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.