rs13075436
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13075436(C;C) |
Make rs13075436(C;T) |
Make rs13075436(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 127242305 |
is a | snp |
is | mentioned by |
dbSNP | rs13075436 |
dbSNP (classic) | rs13075436 |
ClinGen | rs13075436 |
ebi | rs13075436 |
HLI | rs13075436 |
Exac | rs13075436 |
Gnomad | rs13075436 |
Varsome | rs13075436 |
LitVar | rs13075436 |
Map | rs13075436 |
PheGenI | rs13075436 |
Biobank | rs13075436 |
1000 genomes | rs13075436 |
hgdp | rs13075436 |
ensembl | rs13075436 |
geneview | rs13075436 |
scholar | rs13075436 |
rs13075436 | |
pharmgkb | rs13075436 |
gwascentral | rs13075436 |
openSNP | rs13075436 |
23andMe | rs13075436 |
SNPshot | rs13075436 |
SNPdbe | rs13075436 |
MSV3d | rs13075436 |
GWAS Ctlg | rs13075436 |
GMAF | 0.2938 |
Max Magnitude | 0 |
? | (C;C) (C;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 | C |
P-val | 0.000006 |
Odds Ratio | 1.3000 None |