rs9375225
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9375225(G;G) |
Make rs9375225(G;T) |
Make rs9375225(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 98140878 |
is a | snp |
is | mentioned by |
dbSNP | rs9375225 |
dbSNP (classic) | rs9375225 |
ClinGen | rs9375225 |
ebi | rs9375225 |
HLI | rs9375225 |
Exac | rs9375225 |
Gnomad | rs9375225 |
Varsome | rs9375225 |
LitVar | rs9375225 |
Map | rs9375225 |
PheGenI | rs9375225 |
Biobank | rs9375225 |
1000 genomes | rs9375225 |
hgdp | rs9375225 |
ensembl | rs9375225 |
geneview | rs9375225 |
scholar | rs9375225 |
rs9375225 | |
pharmgkb | rs9375225 |
gwascentral | rs9375225 |
openSNP | rs9375225 |
23andMe | rs9375225 |
SNPshot | rs9375225 |
SNPdbe | rs9375225 |
MSV3d | rs9375225 |
GWAS Ctlg | rs9375225 |
GMAF | 0.4045 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23459443] |
Trait | QT interval (interaction) |
Title | Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval. |
Risk Allele | T |
P-val | 6E-6 |
Odds Ratio | NR NR |