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rs61839660

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs61839660(C;T)
Make rs61839660(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position6052734
GeneIL2RA
is asnp
is mentioned by
dbSNPrs61839660
ebirs61839660
HLIrs61839660
Exacrs61839660
Varsomers61839660
Maprs61839660
PheGenIrs61839660
hapmaprs61839660
1000 genomesrs61839660
hgdprs61839660
ensemblrs61839660
gopubmedrs61839660
geneviewrs61839660
scholarrs61839660
googlers61839660
pharmgkbrs61839660
gwascentralrs61839660
openSNPrs61839660
23andMers61839660
23andMe allrs61839660
SNP Nexus

SNPshotrs61839660
SNPdbers61839660
MSV3drs61839660
GWAS Ctlgrs61839660
GMAF0.03398
Max Magnitude0
GWAS snp
PMID [PMID 22293688OA-icon.png]
Trait
Title 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.
Risk Allele
P-val 5E-9
Odds Ratio 1.6000 None