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rs10167219

From SNPedia

Orientationplus
Stabilizedplus
Make rs10167219(C;C)
Make rs10167219(C;T)
Make rs10167219(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position226275057
is asnp
is mentioned by
dbSNPrs10167219
ebirs10167219
HLIrs10167219
Exacrs10167219
Varsomers10167219
Maprs10167219
PheGenIrs10167219
hapmaprs10167219
1000 genomesrs10167219
hgdprs10167219
ensemblrs10167219
gopubmedrs10167219
geneviewrs10167219
scholarrs10167219
googlers10167219
pharmgkbrs10167219
gwascentralrs10167219
openSNPrs10167219
23andMers10167219
23andMe allrs10167219
SNP Nexus

SNPshotrs10167219
SNPdbers10167219
MSV3drs10167219
GWAS Ctlgrs10167219
GMAF0.2704
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23659870OA-icon.png] Common variants in and near IRS1 and subclinical cardiovascular disease in the Framingham Heart Study