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rs6924995

From SNPedia

Orientationplus
Stabilizedplus
Make rs6924995(A;A)
Make rs6924995(A;G)
Make rs6924995(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position16161194
GeneLOC107986517
is asnp
is mentioned by
dbSNPrs6924995
dbSNP (classic)rs6924995
ClinGenrs6924995
ebirs6924995
HLIrs6924995
Exacrs6924995
Gnomadrs6924995
Varsomers6924995
LitVarrs6924995
Maprs6924995
PheGenIrs6924995
Biobankrs6924995
1000 genomesrs6924995
hgdprs6924995
ensemblrs6924995
geneviewrs6924995
scholarrs6924995
googlers6924995
pharmgkbrs6924995
gwascentralrs6924995
openSNPrs6924995
23andMers6924995
SNPshotrs6924995
SNPdbers6924995
MSV3drs6924995
GWAS Ctlgrs6924995
GMAF0.4601
Max Magnitude0
? (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 23100282OA-icon.png] Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study.


[PMID 27071970OA-icon.png] RP1-13D10.2 Is a Novel Modulator of Statin-Induced Changes in Cholesterol