rs2166775
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2166775(A;A) |
Make rs2166775(A;G) |
Make rs2166775(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 143785691 |
Gene | SLC9A9 |
is a | snp |
is | mentioned by |
dbSNP | rs2166775 |
dbSNP (classic) | rs2166775 |
ClinGen | rs2166775 |
ebi | rs2166775 |
HLI | rs2166775 |
Exac | rs2166775 |
Gnomad | rs2166775 |
Varsome | rs2166775 |
LitVar | rs2166775 |
Map | rs2166775 |
PheGenI | rs2166775 |
Biobank | rs2166775 |
1000 genomes | rs2166775 |
hgdp | rs2166775 |
ensembl | rs2166775 |
geneview | rs2166775 |
scholar | rs2166775 |
rs2166775 | |
pharmgkb | rs2166775 |
gwascentral | rs2166775 |
openSNP | rs2166775 |
23andMe | rs2166775 |
SNPshot | rs2166775 |
SNPdbe | rs2166775 |
MSV3d | rs2166775 |
GWAS Ctlg | rs2166775 |
GMAF | 0.3926 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | G |
P-val | 0.000003 |
Odds Ratio | 0.9900 None |