rs10918859
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10918859(A;A) |
Make rs10918859(A;G) |
Make rs10918859(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 162199478 |
Gene | NOS1AP |
is a | snp |
is | mentioned by |
dbSNP | rs10918859 |
dbSNP (classic) | rs10918859 |
ClinGen | rs10918859 |
ebi | rs10918859 |
HLI | rs10918859 |
Exac | rs10918859 |
Gnomad | rs10918859 |
Varsome | rs10918859 |
LitVar | rs10918859 |
Map | rs10918859 |
PheGenI | rs10918859 |
Biobank | rs10918859 |
1000 genomes | rs10918859 |
hgdp | rs10918859 |
ensembl | rs10918859 |
geneview | rs10918859 |
scholar | rs10918859 |
rs10918859 | |
pharmgkb | rs10918859 |
gwascentral | rs10918859 |
openSNP | rs10918859 |
23andMe | rs10918859 |
SNPshot | rs10918859 |
SNPdbe | rs10918859 |
MSV3d | rs10918859 |
GWAS Ctlg | rs10918859 |
GMAF | 0.2103 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21685173] Common Variants in CASQ2, GPD1L and NOS1AP Are Significantly Associated with Risk of Sudden Death in Patients with Coronary Artery Disease
[PMID 23171141] Positive association between rs10918859 of the NOS1AP gene and coronary heart disease in male Han Chinese.