rs11771443
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11771443(C;C) |
Make rs11771443(C;T) |
Make rs11771443(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 150990599 |
Gene | NOS3 |
is a | snp |
is | mentioned by |
dbSNP | rs11771443 |
dbSNP (classic) | rs11771443 |
ClinGen | rs11771443 |
ebi | rs11771443 |
HLI | rs11771443 |
Exac | rs11771443 |
Gnomad | rs11771443 |
Varsome | rs11771443 |
LitVar | rs11771443 |
Map | rs11771443 |
PheGenI | rs11771443 |
Biobank | rs11771443 |
1000 genomes | rs11771443 |
hgdp | rs11771443 |
ensembl | rs11771443 |
geneview | rs11771443 |
scholar | rs11771443 |
rs11771443 | |
pharmgkb | rs11771443 |
gwascentral | rs11771443 |
openSNP | rs11771443 |
23andMe | rs11771443 |
SNPshot | rs11771443 |
SNPdbe | rs11771443 |
MSV3d | rs11771443 |
GWAS Ctlg | rs11771443 |
GMAF | 0.2319 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20409549] NOS3 gene polymorphisms are associated with risk markers of cardiovascular disease, and interact with omega-3 polyunsaturated fatty acids
[PMID 21245953] Association of genetic polymorphisms of eNOS with glaucoma.
[PMID 24085449] Polymorphisms in the endothelial nitric oxide synthase gene associated with recurrent miscarriage
[PMID 27706723] Association between functional polymorphisms in the nitric oxide synthase 3 gene and pediatric acute respiratory distress syndrome.