Tag
Energy Metabolism
79 genetic variants with this tag.
| RSID | Gene | Description | Category | ||
|---|---|---|---|---|---|
| rs11235972 | UCP3 | Intronic UCP3 variant associated with skeletal muscle fat oxidation capacity,... | Liver Fat | Moderate | |
| rs10515237 | PCSK1 PCSK1 A/G (rs10515237) | Intronic variant in PCSK1 that tags the Q665E-S690T functional haplotype, red... | Appetite & Obesity | Moderate | |
| rs1064608 | MTCH2 Pro290Ala | Missense variant in MTCH2 that reduces mitochondrial metabolic efficiency, in... | Hormones & Sleep | Moderate | |
| rs118204015 | ACADVL | Likely-pathogenic VLCAD missense variant abolishing enzyme activity — carrier... | Liver Fat | Strong | |
| rs115532916 | ACAD9 ACAD9 Ala326Pro | Pathogenic missense variant in acyl-CoA dehydrogenase family member 9, causin... | Metabolic Enzymes & Rare Disorders | Strong | |
| rs118204017 | ACADVL | ACADVL missense variant (p.Phe458Leu) classified likely pathogenic for VLCAD ... | Liver Fat | Strong | |
| rs1044498 | ENPP1 K121Q | ENPP1 K121Q variant that increases ENPP1 binding affinity to the insulin rece... | Blood Sugar & Diabetes | Strong | |
| rs10838738 | MTCH2 | Intronic GWAS obesity variant in MTCH2 — affects mitochondrial energy balance... | Appetite & Obesity | Moderate | |
| rs104894005 | GCK Glu279Ter (MODY2) | Pathogenic glucokinase nonsense variant introducing a premature stop codon th... | Blood Sugar & Diabetes | Established | |
| rs119103258 | PYGM | Pathogenic missense variant in muscle glycogen phosphorylase causing post-tra... | Metabolic Enzymes & Rare Disorders | Established | |
| rs11037909 | EXT2 | Intronic EXT2 variant associated with a modest increase in type 2 diabetes su... | Appetite & Obesity | Moderate | |
| rs121434280 | ACADM ACADM Y67H | Pathogenic missense variant in the MCAD enzyme causing a temperature-sensitiv... | Metabolic Enzymes & Rare Disorders | Strong | |
| rs104894008 | GCK Gly261Arg (MODY2) | Pathogenic glucokinase missense variant that nearly abolishes enzyme activity... | Blood Sugar & Diabetes | Established | |
| rs121434281 | ACADM S245L | Rare pathogenic missense variant in the ACADM gene (p.Ser245Leu) causing medi... | Metabolic Enzymes & Rare Disorders | Established | |
| rs104894009 | GCK Arg191Trp (MODY2) | Pathogenic glucokinase missense variant that raises the beta-cell glucose sen... | Blood Sugar & Diabetes | Established | |
| rs11061946 | ADIPOR2 | Intronic variant in the adiponectin receptor 2 gene; rare homozygotes showed ... | Fat Storage & Energy | Emerging | |
| rs121434282 | ACADM Arg281Thr | Pathogenic missense variant in the MCAD enzyme causing medium-chain acyl-CoA ... | Metabolic Enzymes & Rare Disorders | Established | |
| rs121434369 | GCDH R402W (Arg402Trp) | Most common European allele for glutaric acidemia type 1; complete loss of GC... | Metabolic Enzymes & Rare Disorders | Established | |
| rs12640088 | PPARGC1A | Intronic variant in PPARGC1A that may modulate PGC-1alpha expression and mito... | Fitness & Body | Emerging | |
| rs10811661 | CDKN2B | Regulatory variant upstream of CDKN2A/CDKN2B at the 9p21 locus; the T risk al... | Blood Sugar & Diabetes | Strong | |
| rs1152003 | PPARG | PPARG 3'-flanking region variant — the G allele independently tags a PPARG re... | Fat Storage & Energy | Emerging | |
| rs10885406 | TCF7L2 TCF7L2 Wnt Signaling Depth Variant | Intronic TCF7L2 variant tagging the diabetes-risk haplotype and associated wi... | Blood Sugar & Diabetes | Moderate | |
| rs116862713 | PRKAB1 | Rare AMPK beta-1 subunit variant linking central energy sensing to shared mig... | Fat Storage & Energy | Emerging | |
| rs137852769 | HADHA p.Glu510Gln | Most common LCHAD deficiency variant; homozygosity causes severe mitochondria... | Metabolic Enzymes & Rare Disorders | Established | |
| rs10954640 | ENPP1 ENPP1 3'UTR Variant | Intergenic variant near ENPP1-associated regulatory loci; T allele is associa... | Blood Sugar & Diabetes | Emerging | |
| rs515726176 | CPT2 | Rare CPT2 missense variant (p.Arg382Thr) that reduces carnitine palmitoyltran... | Liver Fat | Moderate | |
| rs1143699 | PTPRS PTPRS C/T (rs1143699) | Synonymous PTPRS variant associated with increased type 2 diabetes risk in me... | Blood Sugar & Diabetes | Moderate | |
| rs1175544 | PPARG PPARG rs1175544 | Intronic PPARG variant that accounts for ~7% of individual variation in body ... | Fat Storage & Energy | Emerging | |
| rs142967670 | GCDH R88C | Pathogenic missense variant in glutaryl-CoA dehydrogenase; homozygosity cause... | Metabolic Enzymes & Rare Disorders | Established | |
| rs184660829 | DENND2C | Rare intronic variant near a DENND2C splice site associated with an 8-fold in... | Appetite & Obesity | Moderate | |
| rs12094543 | ZMYM4 ZMYM4 rs12094543 | Intronic variant in ZMYM4, a chromatin-remodeling transcription factor whose ... | Fat Storage & Energy | Emerging | |
| rs1799958 | ACADS G209S (c.625G>A) | Common missense variant in ACADS encoding short-chain acyl-CoA dehydrogenase;... | Metabolic Enzymes & Rare Disorders | Established | |
| rs1943226 | MC4R MC4R third tagSNP | Upstream regulatory tag variant ~3 kb proximal to MC4R, included in MC4R hapl... | Appetite & Obesity | Emerging | |
| rs11705701 | IGF2BP2 IGF2BP2 Insulin Signaling Variant | Upstream regulatory variant in IGF2BP2 that shifts mRNA isoform balance in ad... | Blood Sugar & Diabetes | Moderate | |
| rs12304921 | SLC11A2 | Intronic variant in SLC11A2 (DMT1), the primary intestinal iron transporter, ... | Fat Storage & Energy | Emerging | |
| rs17602729 | AMPD1 C34T (Q12X) | Enzyme critical for energy production during high-intensity exercise; deficie... | Fitness & Body | Strong | |
| rs11708067 | ADCY5 ADCY5 Glucose Signaling Variant | Intronic regulatory variant that reduces ADCY5 expression in pancreatic islet... | Blood Sugar & Diabetes | Strong | |
| rs6536991 | UCP1 | Intronic UCP1 variant — the C allele is associated with reduced overweight ri... | Liver Fat | Emerging | |
| rs12243326 | TCF7L2 TCF7L2 Incretin Response Depth Variant | Intronic TCF7L2 depth variant replicated across multiple populations as a sec... | Blood Sugar & Diabetes | Moderate | |
| rs200788251 | ACADVL ACADVL p.Gly289Arg | Pathogenic missense variant in ACADVL encoding VLCAD; heterozygous carriers a... | Metabolic Enzymes & Rare Disorders | Established | |
| rs13412852 | LPIN1 | Intronic variant in LPIN1 (lipin-1) associated with liver fat accumulation an... | Fat Storage & Energy | Emerging | |
| rs201065226 | CPT2 p.Arg124Ter (R124X) | Rare stop-gain variant in CPT2 abolishing carnitine palmitoyltransferase II, ... | Metabolic Enzymes & Rare Disorders | Strong | |
| rs2867125 | TMEM18 TMEM18 regulatory variant (2p25.3) | Regulatory variant at the TMEM18 locus on chromosome 2p25.3 — one of the most... | Appetite & Obesity | Strong | |
| rs12610022 | INSR | Intronic INSR variant that may alter insulin receptor expression or isoform b... | Blood Sugar & Diabetes | Emerging | |
| rs2034650 | IVD | Intronic regulatory variant in IVD (isovaleryl-CoA dehydrogenase) associated ... | Metabolic Enzymes & Rare Disorders | Emerging | |
| rs17036314 | PPARG | Intronic PPARG variant — carriers of the C allele have elevated fasting gluco... | Fat Storage & Energy | Moderate | |
| rs267606898 | MT-ND5 | Heteroplasmic missense variant in the mitochondrially encoded ND5 subunit of ... | Metabolic Enzymes & Rare Disorders | Strong | |
| rs1402837 | G6PC2 G6PC2 Fasting Glucose Variant | Upstream regulatory variant in G6PC2 that modulates pancreatic beta-cell gluc... | Blood Sugar & Diabetes | Strong | |
| rs267606993 | PYGM PYGM Met1Val (start-loss) | Pathogenic start-codon variant in muscle glycogen phosphorylase; homozygous o... | Metabolic Enzymes & Rare Disorders | Established | |
| rs1571583 | GLIS3 GLIS3 Beta Cell Development Variant | Intronic GLIS3 variant in which the rare A allele modestly elevates TSH, refl... | Blood Sugar & Diabetes | Strong | |
| rs6232 | PCSK1 PCSK1 N221D (Asn221Asp) | Missense variant in PCSK1 encoding an Asn221Asp substitution near the Ca-1 ca... | Appetite & Obesity | Strong | |
| rs6234 | PCSK1 PCSK1 Q665E (Gln665Glu) | Missense variant in PCSK1 that causes a Gln665Glu substitution in the C-termi... | Appetite & Obesity | Strong | |
| rs377022708 | ACAD9 Arg532Trp (R532W) | Pathogenic missense variant in the ACAD9 complex I assembly factor causing se... | Metabolic Enzymes & Rare Disorders | Strong | |
| rs6235 | PCSK1 PCSK1 S690T (Ser690Thr) | Missense variant encoding the Ser690Thr substitution in the C-terminal domain... | Appetite & Obesity | Strong | |
| rs1799999 | PPP1R3A Asp905Tyr | Missense variant in the skeletal muscle glycogen-targeting subunit of protein... | Blood Sugar & Diabetes | Moderate | |
| rs2279525 | PPARGC1A PPARGC1A 3' UTR metabolic association variant | 3' UTR variant in the PGC-1alpha gene that may alter PPARGC1A mRNA stability ... | Fat Storage & Energy | Emerging | |
| rs387906249 | ACADVL c.343del (p.Glu115Lysfs*2) | Pathogenic ACADVL frameshift deletion causing premature protein truncation; h... | Metabolic Enzymes & Rare Disorders | Established | |
| rs66791338 | IVD 5-bp IVD regulatory region indel | Intronic 5-bp indel (AAAGG) in the IVD regulatory region that is the primary ... | Metabolic Enzymes & Rare Disorders | Moderate | |
| rs1801278 | IRS1 Gly972Arg (G972R) | Missense variant in insulin receptor substrate 1 that impairs tyrosine phosph... | Blood Sugar & Diabetes | Strong | |
| rs1884613 | HNF4A HNF4A P2 Promoter T2D Variant | Intronic variant tagging the HNF4A P2 promoter risk haplotype; the G allele s... | Blood Sugar & Diabetes | Moderate | |
| rs74315294 | CPT2 p.Ser113Leu (S113L) | Missense variant in CPT2 that destabilizes the carnitine palmitoyltransferase... | Metabolic Enzymes & Rare Disorders | Established | |
| rs2233580 | PAX4 Arg192His | Missense variant that impairs PAX4's ability to repress insulin and glucagon ... | Blood Sugar & Diabetes | Strong | |
| rs2959272 | PPARG PPARG intronic calorie-restriction trial variant | Intronic PPARG variant significantly associated with individual variation in ... | Fat Storage & Energy | Emerging | |
| rs2237886 | KCNQ1 KCNQ1 Potassium Channel Diabetes Variant | Intronic variant in KCNQ1's imprinted region, tagging the same LD block as es... | Blood Sugar & Diabetes | Moderate | |
| rs358806 | WNT5A | Regulatory variant near WNT5A linked to type 2 diabetes risk via impaired Wnt... | Fat Storage & Energy | Moderate | |
| rs8087522 | MC4R MC4R A/G (rs8087522) | Upstream regulatory variant near MC4R that may create a transcription factor ... | Appetite & Obesity | Emerging | |
| rs3734254 | PPARD T+294C | PPARD 3'UTR variant that reduces fatty acid oxidation capacity and blunts the... | Fat Storage & Energy | Moderate | |
| rs2295490 | TRIB3 Q84R | TRIB3 pseudokinase missense variant that increases Akt inhibition, impairing ... | Blood Sugar & Diabetes | Strong | |
| rs77931234 | ACADM c.985A>G (p.Lys329Glu) | Pathogenic missense variant in ACADM reducing MCAD enzyme activity, predispos... | Cardiomyopathy & Structural Heart | Established | |
| rs397514580 | GCK GCK MODY2 E339K | Pathogenic glucokinase missense variant causing maturity-onset diabetes of th... | Blood Sugar & Diabetes | Strong | |
| rs4607517 | GCK GCK fasting glucose GWAS variant | Common intronic variant near glucokinase that raises fasting glucose by impai... | Blood Sugar & Diabetes | Strong | |
| rs6981587 | ANK1 ANK1 small-ankyrin T2D locus variant | Intronic ANK1 variant at the NKX6-3/ANK1 type 2 diabetes locus; the T allele ... | Fat Storage & Energy | Moderate | |
| rs4812829 | HNF4A HNF4A Intronic T2D Risk Variant | Common intronic variant in HNF4A associated with modestly elevated type 2 dia... | Blood Sugar & Diabetes | Strong | |
| rs6017340 | HNF4A HNF4A Regulatory Variant | Intronic HNF4A tag SNP associated with altered bile acid synthesis regulation... | Blood Sugar & Diabetes | Emerging | |
| rs6031551 | HNF4A HNF4A Regulatory Variant | Intronic variant 80 bp from rs6031552 within the HNF4A P2 promoter haplotype ... | Blood Sugar & Diabetes | Emerging | |
| rs6031552 | HNF4A HNF4A Regulatory Variant | Intronic variant tagging the HNF4A P2 promoter haplotype; carriers have modes... | Blood Sugar & Diabetes | Moderate | |
| rs56051278 | GPD2 | Intronic variant in GPD2 (mitochondrial glycerol-3-phosphate dehydrogenase), ... | Neurology & Cognition | Strong | |
| rs7202877 | CTRB1 | Intergenic variant near CTRB1/CTRB2 that regulates chymotrypsinogen expressio... | Blood Sugar & Diabetes | Strong | |
| rs914458 | PTPN1 PTPN1 downstream variant | Downstream regulatory variant 10 kb 3' of PTPN1 (PTP1B) associated with type ... | Blood Sugar & Diabetes | Emerging |