rs16890196
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs16890196(A;G) |
Make rs16890196(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 32739555 |
Gene | NPR3 |
is a | snp |
is | mentioned by |
dbSNP | rs16890196 |
dbSNP (classic) | rs16890196 |
ClinGen | rs16890196 |
ebi | rs16890196 |
HLI | rs16890196 |
Exac | rs16890196 |
Gnomad | rs16890196 |
Varsome | rs16890196 |
LitVar | rs16890196 |
Map | rs16890196 |
PheGenI | rs16890196 |
Biobank | rs16890196 |
1000 genomes | rs16890196 |
hgdp | rs16890196 |
ensembl | rs16890196 |
geneview | rs16890196 |
scholar | rs16890196 |
rs16890196 | |
pharmgkb | rs16890196 |
gwascentral | rs16890196 |
openSNP | rs16890196 |
23andMe | rs16890196 |
SNPshot | rs16890196 |
SNPdbe | rs16890196 |
MSV3d | rs16890196 |
GWAS Ctlg | rs16890196 |
GMAF | 0.2089 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19326473] Natriuretic peptide system gene variants are associated with ventricular dysfunction after coronary artery bypass grafting.