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rs9806366

From SNPedia

Orientationplus
Stabilizedplus
Make rs9806366(C;C)
Make rs9806366(C;T)
Make rs9806366(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position101262752
is asnp
is mentioned by
dbSNPrs9806366
ebirs9806366
HLIrs9806366
Exacrs9806366
Varsomers9806366
Maprs9806366
PheGenIrs9806366
hapmaprs9806366
1000 genomesrs9806366
hgdprs9806366
ensemblrs9806366
gopubmedrs9806366
geneviewrs9806366
scholarrs9806366
googlers9806366
pharmgkbrs9806366
gwascentralrs9806366
openSNPrs9806366
23andMers9806366
23andMe allrs9806366
SNP Nexus

SNPshotrs9806366
SNPdbers9806366
MSV3drs9806366
GWAS Ctlgrs9806366
GMAF0.1864
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23161441OA-icon.png] Polymorphisms in the Selenoprotein S gene and subclinical cardiovascular disease in the Diabetes Heart Study