rs10800397
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10800397(C;C) |
Make rs10800397(C;T) |
Make rs10800397(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 162267300 |
Gene | NOS1AP |
is a | snp |
is | mentioned by |
dbSNP | rs10800397 |
dbSNP (classic) | rs10800397 |
ClinGen | rs10800397 |
ebi | rs10800397 |
HLI | rs10800397 |
Exac | rs10800397 |
Gnomad | rs10800397 |
Varsome | rs10800397 |
LitVar | rs10800397 |
Map | rs10800397 |
PheGenI | rs10800397 |
Biobank | rs10800397 |
1000 genomes | rs10800397 |
hgdp | rs10800397 |
ensembl | rs10800397 |
geneview | rs10800397 |
scholar | rs10800397 |
rs10800397 | |
pharmgkb | rs10800397 |
gwascentral | rs10800397 |
openSNP | rs10800397 |
23andMe | rs10800397 |
SNPshot | rs10800397 |
SNPdbe | rs10800397 |
MSV3d | rs10800397 |
GWAS Ctlg | rs10800397 |
GMAF | 0.3104 |
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