Research
Tag

Statins

33 genetic variants with this tag.

RSID Gene Description Category
rs11591147 PCSK9 R46L Loss-of-function variant that naturally lowers LDL cholesterol by 15-28% and ... Atherogenic Lipoproteins Established
rs12487736 SCAP SCAP Val798Ile Missense variant in the SCAP cholesterol-sensor gene (Val798Ile); the C allel... Atherogenic Lipoproteins Moderate
rs137852912 PCSK9 D374Y The most severe gain-of-function PCSK9 mutation, increasing LDLR-binding affi... Atherogenic Lipoproteins Established
rs1125226 CYP7A1 CYP7A1 upstream promoter variant Upstream regulatory variant in CYP7A1 that tags haplotypes affecting bile aci... Cholesterol & Lipoproteins Emerging
rs28942111 PCSK9 S127R Gain-of-function PCSK9 missense variant (Ser127Arg) causing autosomal dominan... Atherogenic Lipoproteins Established
rs12721627 CYP3A4 *16 Missense variant reducing CYP3A4 enzyme activity by 50–74% depending on subst... Pharmacogenomics Moderate
rs505151 PCSK9 E670G Common missense variant in PCSK9 exon 12 where the rare G allele raises LDL c... Atherogenic Lipoproteins Moderate
rs12713559 APOB APOB R3558C Rare APOB missense variant reducing LDL-receptor binding affinity by ~40-50%,... Cholesterol & Lipoproteins Moderate
rs137943601 LDLR LDLR E408* (Glu408Ter) Nonsense mutation in the LDLR gene creating a premature stop codon at positio... Cholesterol & Lipoproteins Strong
rs20455 KIF6 Trp719Arg Missense variant in kinesin family member 6; the Arg allele was associated wi... Coronary Artery Disease & Atherosclerosis Moderate
rs5925 LDLR LDLR Expression Co-variant Synonymous variant in LDLR exon 13 that modulates mRNA splicing efficiency in... Atherogenic Lipoproteins Moderate
rs6008845 PPARA PPARA intronic C/T Regulatory PPARA variant where TT homozygotes with type 2 diabetes experience... Atherogenic Lipoproteins Strong
rs185392267 PCSK9 Arg96Cys Gain-of-function missense variant in PCSK9 that increases intracellular LDL r... Cholesterol & Lipoproteins Strong
rs6511720 LDLR Intron 1 Common regulatory variant in the LDL receptor gene affecting LDLR expression,... Atherogenic Lipoproteins Strong
rs2228314 SREBF2 SREBF2 G1784C Missense variant in the master cholesterol transcription factor SREBP-2 that ... Cholesterol & Lipoproteins Moderate
rs688 LDLR Asn591Asn (c.1773C>T) Synonymous LDLR variant that disrupts exon 12 splicing, reduces LDL receptor ... Atherogenic Lipoproteins Strong
rs730882094 LDLR Asn316Ser (N316S) Rare likely-pathogenic missense variant in the LDLR EGF-like repeat domain ca... Atherogenic Lipoproteins Strong
rs28942083 LDLR Cys667Tyr Pathogenic LDLR missense variant abolishing LDL receptor surface expression, ... Cholesterol & Lipoproteins Established
rs730882105 LDLR p.Val524Met Rare LDLR missense variant (c.1570G>A, p.Val524Met) associated with familial ... Atherogenic Lipoproteins Moderate
rs28942084 LDLR LDLR Pro685Leu Pathogenic LDLR missense variant in the EGF precursor domain causing familial... Cholesterol & Lipoproteins Established
rs763625913 LDLR Q770* (c.2308C>T) Rare pathogenic nonsense variant in the LDL receptor gene that abolishes rece... Atherogenic Lipoproteins Established
rs28942085 LDLR LDLR Y828C (J.D. mutation) Pathogenic LDLR missense variant (p.Tyr828Cys) that traps LDL receptors outsi... Cholesterol & Lipoproteins Established
rs3846662 HMGCR HMGCR Intron 13 Splice Variant Intronic HMGCR variant that modulates alternative splicing of exon 13, produc... Cholesterol & Lipoproteins Moderate
rs3846663 HMGCR HMGCR Exon 13 Haplotype Tag Intronic HMGCR variant that tags a haplotype influencing exon 13 alternative ... Cholesterol & Lipoproteins Strong
rs2231142 ABCG2 Q141K Reduces ABCG2 transporter function affecting rosuvastatin levels and uric aci... Pharmacogenomics Established
rs2242480 CYP3A4 *1G Intronic variant in CYP3A4 intron 10 that upregulates a suppressive lncRNA, r... Pharmacogenomics Strong
rs673548 APOB Intronic APOB variant associated with modest differences in apolipoprotein B ... Cholesterol & Lipoproteins Moderate
rs8192870 CYP7A1 CYP7A1 intron 1 variant Intronic variant in the rate-limiting bile acid synthesis gene; T allele carr... Cholesterol & Lipoproteins Moderate
rs9818870 MRAS 3' UTR variant near miRNA binding sites in MRAS, associated with ~15% increas... Coronary Artery Disease & Atherosclerosis Strong
rs35599367 CYP3A4 *22 Intronic splice variant causing ~50% reduced CYP3A4 mRNA expression, affectin... Pharmacogenomics Established
rs4148323 UGT1A1 *6 Gly71Arg Phase II glucuronidation enzyme that metabolizes bilirubin and many drugs inc... Pharmacogenomics Established
rs4149056 SLCO1B1 *5 Statin transport - affects muscle side effect risk with statins Pharmacogenomics Established
rs55785340 CYP3A4 *2 Missense variant reducing CYP3A4-mediated nifedipine clearance, causing eleva... Pharmacogenomics Moderate