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rs11256313

From SNPedia

Orientationplus
Stabilizedplus
Make rs11256313(A;A)
Make rs11256313(A;G)
Make rs11256313(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position6008329
is asnp
is mentioned by
dbSNPrs11256313
ebirs11256313
HLIrs11256313
Exacrs11256313
Varsomers11256313
Maprs11256313
PheGenIrs11256313
hapmaprs11256313
1000 genomesrs11256313
hgdprs11256313
ensemblrs11256313
gopubmedrs11256313
geneviewrs11256313
scholarrs11256313
googlers11256313
pharmgkbrs11256313
gwascentralrs11256313
openSNPrs11256313
23andMers11256313
23andMe allrs11256313
SNP Nexus

SNPshotrs11256313
SNPdbers11256313
MSV3drs11256313
GWAS Ctlgrs11256313
GMAF0.1382
Max Magnitude

[PMID 23170961] Dense mapping of IL2RA shows no association with Graves' disease in Chinese Han population