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rs1875620

From SNPedia

Orientationplus
Stabilizedplus
Make rs1875620(A;A)
Make rs1875620(A;G)
Make rs1875620(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position88925144
is asnp
is mentioned by
dbSNPrs1875620
ebirs1875620
HLIrs1875620
Exacrs1875620
Varsomers1875620
Maprs1875620
PheGenIrs1875620
hapmaprs1875620
1000 genomesrs1875620
hgdprs1875620
ensemblrs1875620
gopubmedrs1875620
geneviewrs1875620
scholarrs1875620
googlers1875620
pharmgkbrs1875620
gwascentralrs1875620
openSNPrs1875620
23andMers1875620
23andMe allrs1875620
SNP Nexus

SNPshotrs1875620
SNPdbers1875620
MSV3drs1875620
GWAS Ctlgrs1875620
GMAF0.3705
Max Magnitude
? (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 7E-7
Odds Ratio 2.8000 None