rs4663476
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4663476(G;G) |
Make rs4663476(G;T) |
Make rs4663476(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 234692420 |
Gene | LINC01173 |
is a | snp |
is | mentioned by |
dbSNP | rs4663476 |
dbSNP (classic) | rs4663476 |
ClinGen | rs4663476 |
ebi | rs4663476 |
HLI | rs4663476 |
Exac | rs4663476 |
Gnomad | rs4663476 |
Varsome | rs4663476 |
LitVar | rs4663476 |
Map | rs4663476 |
PheGenI | rs4663476 |
Biobank | rs4663476 |
1000 genomes | rs4663476 |
hgdp | rs4663476 |
ensembl | rs4663476 |
geneview | rs4663476 |
scholar | rs4663476 |
rs4663476 | |
pharmgkb | rs4663476 |
gwascentral | rs4663476 |
openSNP | rs4663476 |
23andMe | rs4663476 |
SNPshot | rs4663476 |
SNPdbe | rs4663476 |
MSV3d | rs4663476 |
GWAS Ctlg | rs4663476 |
GMAF | 0.1947 |
Max Magnitude | 0 |
? | (G;G) (G;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 | G |
P-val | 0.000008 |
Odds Ratio | 1.2300 None |