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rs7579944

From SNPedia

Orientationplus
Stabilizedplus
Make rs7579944(C;C)
Make rs7579944(C;T)
Make rs7579944(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position30222160
is asnp
is mentioned by
dbSNPrs7579944
ebirs7579944
HLIrs7579944
Exacrs7579944
Varsomers7579944
Maprs7579944
PheGenIrs7579944
hapmaprs7579944
1000 genomesrs7579944
hgdprs7579944
ensemblrs7579944
gopubmedrs7579944
geneviewrs7579944
scholarrs7579944
googlers7579944
pharmgkbrs7579944
gwascentralrs7579944
openSNPrs7579944
23andMers7579944
23andMe allrs7579944
SNP Nexus

SNPshotrs7579944
SNPdbers7579944
MSV3drs7579944
GWAS Ctlgrs7579944
GMAF0.4697
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 1E-8
Odds Ratio None None