rs3913363
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3913363(C;C) |
Make rs3913363(C;T) |
Make rs3913363(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 171936113 |
Gene | LOC105374218 |
is a | snp |
is | mentioned by |
dbSNP | rs3913363 |
dbSNP (classic) | rs3913363 |
ClinGen | rs3913363 |
ebi | rs3913363 |
HLI | rs3913363 |
Exac | rs3913363 |
Gnomad | rs3913363 |
Varsome | rs3913363 |
LitVar | rs3913363 |
Map | rs3913363 |
PheGenI | rs3913363 |
Biobank | rs3913363 |
1000 genomes | rs3913363 |
hgdp | rs3913363 |
ensembl | rs3913363 |
geneview | rs3913363 |
scholar | rs3913363 |
rs3913363 | |
pharmgkb | rs3913363 |
gwascentral | rs3913363 |
openSNP | rs3913363 |
23andMe | rs3913363 |
SNPshot | rs3913363 |
SNPdbe | rs3913363 |
MSV3d | rs3913363 |
GWAS Ctlg | rs3913363 |
GMAF | 0.4972 |
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 | T |
P-val | 4E-7 |
Odds Ratio | 1.3000 None |