rs10266483
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10266483(A;A) |
Make rs10266483(A;G) |
Make rs10266483(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 64272953 |
Gene | VN1R39P |
is a | snp |
is | mentioned by |
dbSNP | rs10266483 |
dbSNP (classic) | rs10266483 |
ClinGen | rs10266483 |
ebi | rs10266483 |
HLI | rs10266483 |
Exac | rs10266483 |
Gnomad | rs10266483 |
Varsome | rs10266483 |
LitVar | rs10266483 |
Map | rs10266483 |
PheGenI | rs10266483 |
Biobank | rs10266483 |
1000 genomes | rs10266483 |
hgdp | rs10266483 |
ensembl | rs10266483 |
geneview | rs10266483 |
scholar | rs10266483 |
rs10266483 | |
pharmgkb | rs10266483 |
gwascentral | rs10266483 |
openSNP | rs10266483 |
23andMe | rs10266483 |
SNPshot | rs10266483 |
SNPdbe | rs10266483 |
MSV3d | rs10266483 |
GWAS Ctlg | rs10266483 |
GMAF | 0.3618 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20339536] |
Trait | Response to statin therapy |
Title | Genome-wide association of lipid-lowering response to statins in combined study populations |
Risk Allele | A |
P-val | 0.000008 |
Odds Ratio | None None |