rs12734991
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12734991(C;C) |
Make rs12734991(C;T) |
Make rs12734991(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 162224786 |
Gene | NOS1AP |
is a | snp |
is | mentioned by |
dbSNP | rs12734991 |
dbSNP (classic) | rs12734991 |
ClinGen | rs12734991 |
ebi | rs12734991 |
HLI | rs12734991 |
Exac | rs12734991 |
Gnomad | rs12734991 |
Varsome | rs12734991 |
LitVar | rs12734991 |
Map | rs12734991 |
PheGenI | rs12734991 |
Biobank | rs12734991 |
1000 genomes | rs12734991 |
hgdp | rs12734991 |
ensembl | rs12734991 |
geneview | rs12734991 |
scholar | rs12734991 |
rs12734991 | |
pharmgkb | rs12734991 |
gwascentral | rs12734991 |
openSNP | rs12734991 |
23andMe | rs12734991 |
SNPshot | rs12734991 |
SNPdbe | rs12734991 |
MSV3d | rs12734991 |
GWAS Ctlg | rs12734991 |
GMAF | 0.3466 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22682551] Common Variation in the NOS1AP Gene Is Associated With Drug-Induced QT Prolongation and Ventricular Arrhythmia