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rs10876993

From SNPedia

Orientationplus
Stabilizedplus
Make rs10876993(C;C)
Make rs10876993(C;T)
Make rs10876993(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position57668884
is asnp
is mentioned by
dbSNPrs10876993
ebirs10876993
HLIrs10876993
Exacrs10876993
Varsomers10876993
Maprs10876993
PheGenIrs10876993
hapmaprs10876993
1000 genomesrs10876993
hgdprs10876993
ensemblrs10876993
gopubmedrs10876993
geneviewrs10876993
scholarrs10876993
googlers10876993
pharmgkbrs10876993
gwascentralrs10876993
openSNPrs10876993
23andMers10876993
23andMe allrs10876993
SNP Nexus

SNPshotrs10876993
SNPdbers10876993
MSV3drs10876993
GWAS Ctlgrs10876993
GMAF0.494
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21383967OA-icon.png]
Trait
Title Meta-Analysis of Genome-Wide Association Studies in Celiac Disease and Rheumatoid Arthritis Identifies Fourteen Non-HLA Shared Loci
Risk Allele
P-val 0.000004
Odds Ratio None None