rs9315632
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9315632(G;G) |
Make rs9315632(G;T) |
Make rs9315632(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 38942490 |
is a | snp |
is | mentioned by |
dbSNP | rs9315632 |
dbSNP (classic) | rs9315632 |
ClinGen | rs9315632 |
ebi | rs9315632 |
HLI | rs9315632 |
Exac | rs9315632 |
Gnomad | rs9315632 |
Varsome | rs9315632 |
LitVar | rs9315632 |
Map | rs9315632 |
PheGenI | rs9315632 |
Biobank | rs9315632 |
1000 genomes | rs9315632 |
hgdp | rs9315632 |
ensembl | rs9315632 |
geneview | rs9315632 |
scholar | rs9315632 |
rs9315632 | |
pharmgkb | rs9315632 |
gwascentral | rs9315632 |
openSNP | rs9315632 |
23andMe | rs9315632 |
SNPshot | rs9315632 |
SNPdbe | rs9315632 |
MSV3d | rs9315632 |
GWAS Ctlg | rs9315632 |
GMAF | 0.2645 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20694148] |
Trait | |
Title | A genome-wide association study of the metabolic syndrome in Indian Asian men |
Risk Allele | |
P-val | 0.000003 |
Odds Ratio | None None |