Research
Tag

Lipid Metabolism

54 genetic variants with this tag.

RSID Gene Description Category
rs1044317 ABCG1 ABCG1 3'UTR variant 3'UTR variant in ABCG1 that may reduce transporter expression, impairing chol... Cholesterol & Lipoproteins Moderate
rs1148259 ANKRD30A Synonymous variant in the 3′ UTR of ANKRD30A associated with altered circulat... Metabolic Enzymes & Rare Disorders Emerging
rs12487736 SCAP SCAP Val798Ile Missense variant in the SCAP cholesterol-sensor gene (Val798Ile); the C allel... Atherogenic Lipoproteins Moderate
rs12678919 LPL Intergenic variant 19 kb downstream of lipoprotein lipase (LPL) that tags a r... Triglycerides & Fatty Acids Strong
rs137853964 LDLR Val827Ile / Val827Phe LDLR missense variant at position 827 within the cytoplasmic NPXY internaliza... Atherogenic Lipoproteins Moderate
rs11568822 APOC1 APOC1 HCR-1 promoter variant Promoter insertion variant in APOC1 that increases gene transcription by 50%,... Cholesterol & Lipoproteins Moderate
rs13236689 CD36 Intronic CD36 variant that acts as a platelet eQTL, modulating CD36 surface e... Triglycerides & Fatty Acids Moderate
rs1378577 ABCG1 ABCG1 ischemic stroke variant Regulatory variant ~2kb upstream of ABCG1 that modulates transporter expressi... Atherogenic Lipoproteins Moderate
rs10889160 CYP2J2 Intronic CYP2J2 tag SNP; the C allele marks a haplotype associated with reduc... Vascular Inflammation & Remodeling Moderate
rs1800588 LIPC -514C>T Promoter variant that reduces hepatic lipase activity, raising HDL-C levels b... Atherogenic Lipoproteins Strong
rs1800591 MTTP MTTP -493G/T Promoter-region variant in MTTP that reduces hepatic MTTP transcription; the ... Liver Fat Moderate
rs12740374 SORT1 1p13.3 locus Regulatory variant that increases sortilin expression, lowering LDL cholester... Coronary Artery Disease & Atherosclerosis Established
rs150090666 PDE3B PDE3B R783X Loss-of-function variant in phosphodiesterase 3B — carriers have enhanced cAM... Triglycerides & Fatty Acids Strong
rs199673455 GPD1 Pathogenic missense variant in glycerol-3-phosphate dehydrogenase 1; homozygo... Liver Fat Strong
rs121918385 APOB APOB Glu4034fs Frameshift deletion in APOB that truncates apolipoprotein B, causing familial... Cholesterol & Lipoproteins Strong
rs2972164 PPARG Intronic PPARG variant associated with rate of change in insulin sensitivity ... Liver Fat Moderate
rs4149338 ABCA1 ABCA1 3'UTR Stroke-Associated Variant 3'UTR variant in the ATP-binding cassette transporter A1 gene; the G allele (... Atherogenic Lipoproteins Emerging
rs113809142 ABCA7 ABCA7 splice donor variant (c.4416+2T>G) Rare splice donor variant in ABCA7 that disrupts mRNA processing, causing hap... Neurology & Cognition Strong
rs137853096 HSD17B4 Gly16Ser Pathogenic missense variant in D-bifunctional protein (p.Gly16Ser) disrupting... Metabolic Enzymes & Rare Disorders Established
rs4225 APOC3 APOC3 3'UTR c.*71G>T 3'UTR variant that creates a microRNA-4271 binding site; the T allele suppres... Atherogenic Lipoproteins Moderate
rs4253623 PPARA Intronic PPARA variant whose minor G allele has been associated with modest m... Atherogenic Lipoproteins Emerging
rs505151 PCSK9 E670G Common missense variant in PCSK9 exon 12 where the rare G allele raises LDL c... Atherogenic Lipoproteins Moderate
rs11868035 SREBF1 SREBF1 intronic/3'UTR variant affecting SREBP-1c expression, associated with ... Fat Storage & Energy Moderate
rs613084 CPT1A CPT1A carnitine shuttle variant Intronic variant that influences CPT1A expression and fatty acid oxidation ca... Liver Fat Moderate
rs5177 LRP8 LRP8 3'UTR variant 3'UTR variant in LRP8 (ApoER2) that affects mRNA stability and forms part of ... Atherogenic Lipoproteins Moderate
rs1457043 CYP7A1 Intronic variant in CYP7A1 that tags a haplotype block influencing cholestero... Cholesterol & Lipoproteins Moderate
rs1800775 CETP -629C>A CETP promoter variant that reduces CETP expression via Sp1/Sp3 repression, ra... Cholesterol & Lipoproteins Strong
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
rs2298566 SNX19 Missense variant in sorting nexin 19 that alters endolysosomal positioning at... Coronary Artery Disease & Atherosclerosis Moderate
rs2228314 SREBF2 SREBF2 G1784C Missense variant in the master cholesterol transcription factor SREBP-2 that ... Cholesterol & Lipoproteins Moderate
rs17482753 LPL LPL G>T (Intergenic Variant) Intergenic variant near the lipoprotein lipase gene on 8p21.3 with an indepen... Triglycerides & Fatty Acids Moderate
rs2234714 ABCG1 ABCG1 promoter variant Intronic ABCG1 variant near the promoter region; homozygous carriers of the m... Cholesterol & Lipoproteins Emerging
rs688 LDLR Asn591Asn (c.1773C>T) Synonymous LDLR variant that disrupts exon 12 splicing, reduces LDL receptor ... Atherogenic Lipoproteins Strong
rs2072114 FADS2 FADS2 Intron 1 Variant Intronic FADS2 haplotype tag SNP — the G allele is linked to altered delta-6 ... Triglycerides & Fatty Acids Moderate
rs519664 TTC39B TTC39B rs519664 Intronic variant in TTC39B (9p22) that increases endometriosis susceptibility... Endometriosis & Uterine Health Strong
rs2197076 FABP1 Intronic FABP1 variant associated with type 2 diabetes risk and insulin resis... Triglycerides & Fatty Acids Moderate
rs3846662 HMGCR HMGCR Intron 13 Splice Variant Intronic HMGCR variant that modulates alternative splicing of exon 13, produc... Cholesterol & Lipoproteins Moderate
rs2236212 ELOVL2 Intronic variant in ELOVL2 that reduces elongase-2 enzyme activity, impairing... Triglycerides & Fatty Acids Moderate
rs2297508 SREBF1 SREBF1 G952G SREBF1 3' UTR variant that subtly impairs SREBP-1c function, increasing risk ... Fat Storage & Energy Moderate
rs4900442 CYP46A1 Intronic variant in the brain cholesterol 24-hydroxylase gene; C allele assoc... Cholesterol & Lipoproteins Moderate
rs3211867 CD36 Intronic CD36 variant that reduces CD36 expression, impairing postprandial fa... Triglycerides & Fatty Acids Moderate
rs71785313 APOL1 G2 (del388N389Y) Six-base-pair in-frame deletion removing two amino acids from apolipoprotein ... Cholesterol & Lipoproteins Established
rs3211883 CD36 Intronic CD36 variant associated with altered body adiposity and platelet CD3... Triglycerides & Fatty Acids Moderate
rs3212018 CD36 A 16-bp deletion in the 3' untranslated region of CD36 that may reduce mRNA s... Triglycerides & Fatty Acids Emerging
rs35136575 APOC1P1 HCR-2 Enhancer Variant Regulatory variant in the APOE/APOC hepatic enhancer HCR-2 that lowers plasma... Triglycerides & Fatty Acids Strong
rs8192870 CYP7A1 CYP7A1 intron 1 variant Intronic variant in the rate-limiting bile acid synthesis gene; T allele carr... Cholesterol & Lipoproteins Moderate
rs3734398 ELOVL2 3' UTR variant in the ELOVL2 elongase gene that reduces DHA synthesis from it... Triglycerides & Fatty Acids Strong
rs3816873 MTTP MTTP I128T Missense variant in MTTP (microsomal triglyceride transfer protein) at residu... Fat Storage & Energy Moderate
rs3856806 PPARG His477His (C1431T) Synonymous PPARG variant where the T allele reduces type 2 diabetes risk and ... Fat Storage & Energy Strong
rs5882 CETP I405V Missense variant that reduces CETP enzyme activity, raising HDL-C and enlargi... Longevity & Aging Moderate
rs5181 LRP8 Trp466Cys Rare missense variant in the ApoE receptor 2 (LRP8) ligand-binding domain, di... Fat Storage & Energy Emerging
rs4939883 LOC105372112 Intronic variant near LIPG whose T allele increases circulating endothelial l... Triglycerides & Fatty Acids Strong
rs953413 ELOVL2 Intronic enhancer variant in ELOVL2 that controls transcription factor bindin... Triglycerides & Fatty Acids Strong