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rs4693075

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs4693075(C;C)
Make rs4693075(C;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position83271015
GeneCOQ2
is asnp
is mentioned by
dbSNPrs4693075
ebirs4693075
HLIrs4693075
Exacrs4693075
Varsomers4693075
Maprs4693075
PheGenIrs4693075
hapmaprs4693075
1000 genomesrs4693075
hgdprs4693075
ensemblrs4693075
gopubmedrs4693075
geneviewrs4693075
scholarrs4693075
googlers4693075
pharmgkbrs4693075
gwascentralrs4693075
openSNPrs4693075
23andMers4693075
23andMe allrs4693075
SNP Nexus

SNPshotrs4693075
SNPdbers4693075
MSV3drs4693075
GWAS Ctlgrs4693075
GMAF0.3292
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 23942138OA-icon.png] SLCO1B1 Genetic Variant Associated With Statin-Induced Myopathy: A Proof of Concept Study Using the Clinical Practice Research Datalink (CPRD)


[PMID 19406828OA-icon.png] Inverse correlation between HPSE gene single nucleotide polymorphisms and heparanase expression: possibility of multiple levels of heparanase regulation.


ClinVar
Risk rs4693075(C;C)
Alt rs4693075(C;C)
Reference rs4693075(G;G)
Significance Drug-response
Disease rosuvastatin response - Toxicity/ADR atorvastatin response - Toxicity/ADR hmg coa reductase inhibitors response - Toxicity/ADR
Variation info
Gene COQ2
CLNDBN rosuvastatin response - Toxicity/ADR atorvastatin response - Toxicity/ADR hmg coa reductase inhibitors response - Toxicity/ADR
Reversed 0
HGVS NC_000004.11:g.84192168G>C
CLNSRC PharmGKB Clinical Annotation PharmGKB
CLNACC RCV000211139.1, RCV000211267.1, RCV000211353.1,