rs1009592
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1009592(C;C) |
Make rs1009592(C;G) |
Make rs1009592(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 11868657 |
is a | snp |
is | mentioned by |
dbSNP | rs1009592 |
dbSNP (classic) | rs1009592 |
ClinGen | rs1009592 |
ebi | rs1009592 |
HLI | rs1009592 |
Exac | rs1009592 |
Gnomad | rs1009592 |
Varsome | rs1009592 |
LitVar | rs1009592 |
Map | rs1009592 |
PheGenI | rs1009592 |
Biobank | rs1009592 |
1000 genomes | rs1009592 |
hgdp | rs1009592 |
ensembl | rs1009592 |
geneview | rs1009592 |
scholar | rs1009592 |
rs1009592 | |
pharmgkb | rs1009592 |
gwascentral | rs1009592 |
openSNP | rs1009592 |
23andMe | rs1009592 |
SNPshot | rs1009592 |
SNPdbe | rs1009592 |
MSV3d | rs1009592 |
GWAS Ctlg | rs1009592 |
GMAF | 0.3526 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 19326473] Natriuretic peptide system gene variants are associated with ventricular dysfunction after coronary artery bypass grafting.