rs3918181
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3918181(A;A) |
Make rs3918181(A;G) |
Make rs3918181(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 151004695 |
Gene | NOS3 |
is a | snp |
is | mentioned by |
dbSNP | rs3918181 |
dbSNP (classic) | rs3918181 |
ClinGen | rs3918181 |
ebi | rs3918181 |
HLI | rs3918181 |
Exac | rs3918181 |
Gnomad | rs3918181 |
Varsome | rs3918181 |
LitVar | rs3918181 |
Map | rs3918181 |
PheGenI | rs3918181 |
Biobank | rs3918181 |
1000 genomes | rs3918181 |
hgdp | rs3918181 |
ensembl | rs3918181 |
geneview | rs3918181 |
scholar | rs3918181 |
rs3918181 | |
pharmgkb | rs3918181 |
gwascentral | rs3918181 |
openSNP | rs3918181 |
23andMe | rs3918181 |
SNPshot | rs3918181 |
SNPdbe | rs3918181 |
MSV3d | rs3918181 |
GWAS Ctlg | rs3918181 |
GMAF | 0.2994 |
Max Magnitude | 0 |
[PMID 24213141] A susceptibility haplotype within the endothelial nitric oxide synthase gene influences bone mineral density in hypertensive women [PMID 20428408] A genetic study of the NOS3 gene for ischemic stroke in a Chinese population.