rs790123
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs790123(A;A) |
Make rs790123(A;G) |
Make rs790123(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 122670146 |
is a | snp |
is | mentioned by |
dbSNP | rs790123 |
dbSNP (classic) | rs790123 |
ClinGen | rs790123 |
ebi | rs790123 |
HLI | rs790123 |
Exac | rs790123 |
Gnomad | rs790123 |
Varsome | rs790123 |
LitVar | rs790123 |
Map | rs790123 |
PheGenI | rs790123 |
Biobank | rs790123 |
1000 genomes | rs790123 |
hgdp | rs790123 |
ensembl | rs790123 |
geneview | rs790123 |
scholar | rs790123 |
rs790123 | |
pharmgkb | rs790123 |
gwascentral | rs790123 |
openSNP | rs790123 |
23andMe | rs790123 |
SNPshot | rs790123 |
SNPdbe | rs790123 |
MSV3d | rs790123 |
GWAS Ctlg | rs790123 |
GMAF | 0.4968 |
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 | T |
P-val | 0.000006 |
Odds Ratio | 1.0700 None |