Research
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