rs7168353
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7168353(C;C) |
Make rs7168353(C;G) |
Make rs7168353(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 93095172 |
Gene | LOC101927025 |
is a | snp |
is | mentioned by |
dbSNP | rs7168353 |
dbSNP (classic) | rs7168353 |
ClinGen | rs7168353 |
ebi | rs7168353 |
HLI | rs7168353 |
Exac | rs7168353 |
Gnomad | rs7168353 |
Varsome | rs7168353 |
LitVar | rs7168353 |
Map | rs7168353 |
PheGenI | rs7168353 |
Biobank | rs7168353 |
1000 genomes | rs7168353 |
hgdp | rs7168353 |
ensembl | rs7168353 |
geneview | rs7168353 |
scholar | rs7168353 |
rs7168353 | |
pharmgkb | rs7168353 |
gwascentral | rs7168353 |
openSNP | rs7168353 |
23andMe | rs7168353 |
SNPshot | rs7168353 |
SNPdbe | rs7168353 |
MSV3d | rs7168353 |
GWAS Ctlg | rs7168353 |
GMAF | 0.1713 |
Max Magnitude | 0 |
? | (C;C) (C;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 | C |
P-val | 0.000001 |
Odds Ratio | None None |