rs4265793
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4265793(C;C) |
Make rs4265793(C;T) |
Make rs4265793(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 19017227 |
Gene | TMC7 |
is a | snp |
is | mentioned by |
dbSNP | rs4265793 |
dbSNP (classic) | rs4265793 |
ClinGen | rs4265793 |
ebi | rs4265793 |
HLI | rs4265793 |
Exac | rs4265793 |
Gnomad | rs4265793 |
Varsome | rs4265793 |
LitVar | rs4265793 |
Map | rs4265793 |
PheGenI | rs4265793 |
Biobank | rs4265793 |
1000 genomes | rs4265793 |
hgdp | rs4265793 |
ensembl | rs4265793 |
geneview | rs4265793 |
scholar | rs4265793 |
rs4265793 | |
pharmgkb | rs4265793 |
gwascentral | rs4265793 |
openSNP | rs4265793 |
23andMe | rs4265793 |
SNPshot | rs4265793 |
SNPdbe | rs4265793 |
MSV3d | rs4265793 |
GWAS Ctlg | rs4265793 |
GMAF | 0.09734 |
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 | 0.000006 |
Odds Ratio | 1.2200 None |