rs3767489
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3767489(A;A) |
Make rs3767489(A;G) |
Make rs3767489(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 192746685 |
is a | snp |
is | mentioned by |
dbSNP | rs3767489 |
dbSNP (classic) | rs3767489 |
ClinGen | rs3767489 |
ebi | rs3767489 |
HLI | rs3767489 |
Exac | rs3767489 |
Gnomad | rs3767489 |
Varsome | rs3767489 |
LitVar | rs3767489 |
Map | rs3767489 |
PheGenI | rs3767489 |
Biobank | rs3767489 |
1000 genomes | rs3767489 |
hgdp | rs3767489 |
ensembl | rs3767489 |
geneview | rs3767489 |
scholar | rs3767489 |
rs3767489 | |
pharmgkb | rs3767489 |
gwascentral | rs3767489 |
openSNP | rs3767489 |
23andMe | rs3767489 |
SNPshot | rs3767489 |
SNPdbe | rs3767489 |
MSV3d | rs3767489 |
GWAS Ctlg | rs3767489 |
GMAF | 0.4082 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19927152] Accumulation of common polymorphisms is associated with development of hypertension: a 12-year follow-up from the Ohasama study