rs6924995
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6924995(A;A) |
Make rs6924995(A;G) |
Make rs6924995(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 16161194 |
Gene | LOC107986517 |
is a | snp |
is | mentioned by |
dbSNP | rs6924995 |
dbSNP (classic) | rs6924995 |
ClinGen | rs6924995 |
ebi | rs6924995 |
HLI | rs6924995 |
Exac | rs6924995 |
Gnomad | rs6924995 |
Varsome | rs6924995 |
LitVar | rs6924995 |
Map | rs6924995 |
PheGenI | rs6924995 |
Biobank | rs6924995 |
1000 genomes | rs6924995 |
hgdp | rs6924995 |
ensembl | rs6924995 |
geneview | rs6924995 |
scholar | rs6924995 |
rs6924995 | |
pharmgkb | rs6924995 |
gwascentral | rs6924995 |
openSNP | rs6924995 |
23andMe | rs6924995 |
SNPshot | rs6924995 |
SNPdbe | rs6924995 |
MSV3d | rs6924995 |
GWAS Ctlg | rs6924995 |
GMAF | 0.4601 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22331829] |
Trait | |
Title | Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial. |
Risk Allele | |
P-val | 5E-7 |
Odds Ratio | 4.1000 None |
[PMID 23100282] Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study.
[PMID 27071970] RP1-13D10.2 Is a Novel Modulator of Statin-Induced Changes in Cholesterol