rs4719147
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4719147(G;G) |
Make rs4719147(G;T) |
Make rs4719147(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 71551174 |
Gene | WBSCR17 |
is a | snp |
is | mentioned by |
dbSNP | rs4719147 |
dbSNP (classic) | rs4719147 |
ClinGen | rs4719147 |
ebi | rs4719147 |
HLI | rs4719147 |
Exac | rs4719147 |
Gnomad | rs4719147 |
Varsome | rs4719147 |
LitVar | rs4719147 |
Map | rs4719147 |
PheGenI | rs4719147 |
Biobank | rs4719147 |
1000 genomes | rs4719147 |
hgdp | rs4719147 |
ensembl | rs4719147 |
geneview | rs4719147 |
scholar | rs4719147 |
rs4719147 | |
pharmgkb | rs4719147 |
gwascentral | rs4719147 |
openSNP | rs4719147 |
23andMe | rs4719147 |
SNPshot | rs4719147 |
SNPdbe | rs4719147 |
MSV3d | rs4719147 |
GWAS Ctlg | rs4719147 |
GMAF | 0.4334 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22566498![]() |
Trait | |
Title | Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker. |
Risk Allele | T |
P-val | 0.000002 |
Odds Ratio | 1.1300 None |