rs9806366
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9806366(C;C) |
Make rs9806366(C;T) |
Make rs9806366(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 101262752 |
is a | snp |
is | mentioned by |
dbSNP | rs9806366 |
dbSNP (classic) | rs9806366 |
ClinGen | rs9806366 |
ebi | rs9806366 |
HLI | rs9806366 |
Exac | rs9806366 |
Gnomad | rs9806366 |
Varsome | rs9806366 |
LitVar | rs9806366 |
Map | rs9806366 |
PheGenI | rs9806366 |
Biobank | rs9806366 |
1000 genomes | rs9806366 |
hgdp | rs9806366 |
ensembl | rs9806366 |
geneview | rs9806366 |
scholar | rs9806366 |
rs9806366 | |
pharmgkb | rs9806366 |
gwascentral | rs9806366 |
openSNP | rs9806366 |
23andMe | rs9806366 |
SNPshot | rs9806366 |
SNPdbe | rs9806366 |
MSV3d | rs9806366 |
GWAS Ctlg | rs9806366 |
GMAF | 0.1864 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23161441] Polymorphisms in the Selenoprotein S gene and subclinical cardiovascular disease in the Diabetes Heart Study