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 |