Tag
Metabolic
119 genetic variants with this tag.
| RSID | Gene | Description | Category | ||
|---|---|---|---|---|---|
| rs1000940 | RABEP1 RABEP1 Metabolic-Immune Regulatory Variant | Intronic variant in RABEP1 associated with fasting glucose modulation under p... | Autoimmune Tolerance & T-Cell Regulation | Emerging | |
| rs10010131 | WFS1 WFS1 Intron 4 T2D Risk Variant | Intronic variant in WFS1 (wolframin) on chromosome 4q22, one of the earliest ... | Blood Sugar & Diabetes | Strong | |
| rs1001179 | CAT -262C>T | Catalase promoter variant affecting hydrogen peroxide clearance and antioxida... | Methylation & Detox | Strong | |
| rs113994167 | ACADVL p.Val283Ala (V283A) | Most common VLCAD deficiency variant in the US, causing mild late-onset disea... | Metabolic Enzymes & Rare Disorders | Established | |
| rs1054564 | GDF15 GDF15 3'UTR rs1054564 | 3'UTR variant that controls GDF15 expression via microRNA regulation — C alle... | Endometriosis & Uterine Health | Moderate | |
| rs1064608 | MTCH2 Pro290Ala | Missense variant in MTCH2 that reduces mitochondrial metabolic efficiency, in... | Hormones & Sleep | Moderate | |
| rs1148259 | ANKRD30A | Synonymous variant in the 3′ UTR of ANKRD30A associated with altered circulat... | Metabolic Enzymes & Rare Disorders | Emerging | |
| rs10166942 | TRPM8 | Upstream regulatory variant of the cold-sensing TRPM8 channel that modulates ... | Neurology & Cognition | Strong | |
| rs10838738 | MTCH2 | Intronic GWAS obesity variant in MTCH2 — affects mitochondrial energy balance... | Appetite & Obesity | Moderate | |
| rs10852521 | FTO | FTO intron 1 variant associated with BMI and body fat accumulation, with stro... | Fitness & Body | Moderate | |
| rs118204437 | GALNS Arg386Cys | Pathogenic missense variant abolishing GALNS enzyme activity; biallelic carri... | Metabolic Enzymes & Rare Disorders | Established | |
| rs104894005 | GCK Glu279Ter (MODY2) | Pathogenic glucokinase nonsense variant introducing a premature stop codon th... | Blood Sugar & Diabetes | Established | |
| rs10865710 | PPARG PPARG C-681G | PPARG promoter-region enhancer variant that reduces PPARgamma expression, inc... | Fat Storage & Energy | Moderate | |
| rs10938397 | GNPDA2 | GIANT consortium GWAS obesity locus near GNPDA2 — affects hexosamine-pathway-... | Appetite & Obesity | Strong | |
| rs119103258 | PYGM | Pathogenic missense variant in muscle glycogen phosphorylase causing post-tra... | Metabolic Enzymes & Rare Disorders | Established | |
| rs10882283 | RBP4 RBP4 rs10882283 | 5' UTR variant in RBP4 that influences expression of retinol binding protein ... | Fat Storage & Energy | Moderate | |
| rs121434280 | ACADM ACADM Y67H | Pathogenic missense variant in the MCAD enzyme causing a temperature-sensitiv... | Metabolic Enzymes & Rare Disorders | Strong | |
| rs1800591 | MTTP MTTP -493G/T | Promoter-region variant in MTTP that reduces hepatic MTTP transcription; the ... | Liver Fat | Moderate | |
| 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 | |
| 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 | |
| rs104894009 | GCK Arg191Trp (MODY2) | Pathogenic glucokinase missense variant that raises the beta-cell glucose sen... | Blood Sugar & Diabetes | Established | |
| rs11152221 | MC4R MC4R Proximal LD Block Variant | Intergenic variant in the proximal 3' regulatory block near MC4R associated w... | Appetite & Obesity | Strong | |
| rs121434282 | ACADM Arg281Thr | Pathogenic missense variant in the MCAD enzyme causing medium-chain acyl-CoA ... | Metabolic Enzymes & Rare Disorders | Established | |
| rs11644943 | FTO FTO Mid-Gene Intron Variant | An intronic FTO variant outside the well-known intron-1 obesity cluster; the ... | Appetite & Obesity | Emerging | |
| rs121434369 | GCDH R402W (Arg402Trp) | Most common European allele for glutaric acidemia type 1; complete loss of GC... | Metabolic Enzymes & Rare Disorders | Established | |
| rs10811661 | CDKN2B | Regulatory variant upstream of CDKN2A/CDKN2B at the 9p21 locus; the T risk al... | Blood Sugar & Diabetes | Strong | |
| rs10885122 | ADRA2A ADRA2A Beta-Cell cAMP Variant | Intergenic variant near ADRA2A that modulates alpha-2A adrenergic receptor ex... | Blood Sugar & Diabetes | Moderate | |
| rs12970134 | MC4R MC4R region variant | Near-gene variant ~188kb downstream of MC4R associated with increased waist c... | Appetite & Obesity | Strong | |
| rs13407913 | ADCY3 | Intronic variant in the adenylyl cyclase 3 gene, which encodes a cAMP-produci... | Fitness & Body | Emerging | |
| rs2296241 | CYP24A1 | Synonymous coding variant in CYP24A1 (vitamin D 24-hydroxylase) that tags fun... | Vitamin D Metabolism | Moderate | |
| rs2972164 | PPARG | Intronic PPARG variant associated with rate of change in insulin sensitivity ... | Liver Fat | Moderate | |
| rs137852769 | HADHA p.Glu510Gln | Most common LCHAD deficiency variant; homozygosity causes severe mitochondria... | Metabolic Enzymes & Rare Disorders | Established | |
| rs1420318 | FTO | FTO intron 8 variant associated with nominal spine bone mineral density effec... | Fitness & Body | Emerging | |
| rs17782313 | MC4R Near-gene C>T | Intergenic variant 188kb downstream of MC4R affecting appetite regulation, me... | Appetite & Obesity | Strong | |
| rs1111875 | HHEX HHEX/IDE locus T2D risk variant | Primary tag SNP at the HHEX/IDE locus on chromosome 10q23, one of the earlies... | Blood Sugar & Diabetes | Established | |
| rs1800544 | ADRA2A ADRA2A Promoter -1291C>G | Promoter variant that alters alpha-2A adrenergic receptor expression, affecti... | Appetite & Obesity | Moderate | |
| rs142967670 | GCDH R88C | Pathogenic missense variant in glutaryl-CoA dehydrogenase; homozygosity cause... | Metabolic Enzymes & Rare Disorders | Established | |
| rs199971687 | MMAB | Pathogenic splice acceptor variant in MMAB that abolishes adenosylcobalamin s... | Vitamins & Nutrient Absorption | Established | |
| rs563694 | ABCB11 G6PC2/ABCB11 fasting glucose locus | Intronic variant in ABCB11 in strong linkage disequilibrium with G6PC2 regula... | Liver Fat | Strong | |
| rs146582474 | SLC7A7 | Finnish founder splice acceptor mutation abolishing y+LAT1 transport activity... | Metabolic Enzymes & Rare Disorders | Established | |
| rs2271194 | ERBB3 ERBB3/RAB5B PCOS Metabolic | A splice-region variant at the ERBB3/RAB5B locus on chromosome 12q13.2, a rep... | Fertility & Ovarian Function | Strong | |
| rs58542926 | TM6SF2 E167K | Lipid transport variant that impairs VLDL secretion, creating a paradoxical t... | Liver Fat | Strong | |
| rs12094543 | ZMYM4 ZMYM4 rs12094543 | Intronic variant in ZMYM4, a chromatin-remodeling transcription factor whose ... | Fat Storage & Energy | Emerging | |
| rs17219084 | FTO | FTO intron variant in the extended obesity-associated region, with explorator... | Fitness & Body | 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 | |
| rs1801175 | G6PC1 | Pathogenic missense variant in glucose-6-phosphatase catalytic subunit 1 caus... | Metabolic Enzymes & Rare Disorders | Established | |
| rs2229616 | MC4R V103I | Missense variant in MC4R converting valine to isoleucine at position 103; the... | Appetite & Obesity | Strong | |
| rs1554483 | CLOCK | Intronic CLOCK variant whose G allele, in a haplotype with rs4864548 A, confe... | Hormones & Sleep | Moderate | |
| rs193922339 | GCK | Likely-pathogenic GCK missense variant (p.Phe316Tyr) causing glucokinase loss... | Metabolic Enzymes & Rare Disorders | Strong | |
| rs12243326 | TCF7L2 TCF7L2 Incretin Response Depth Variant | Intronic TCF7L2 depth variant replicated across multiple populations as a sec... | Blood Sugar & Diabetes | Moderate | |
| rs12636454 | PPARG PPARG rs12636454 | Intronic PPARG variant associated with modest reduction in type 2 diabetes ri... | Fat Storage & Energy | Emerging | |
| 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 | |
| rs28941784 | MMAB Arg186Trp (R186W) | Missense variant eliminating MMAB adenosylcobalamin synthase activity; the mo... | Vitamins & Nutrient Absorption | Established | |
| rs12610022 | INSR | Intronic INSR variant that may alter insulin receptor expression or isoform b... | Blood Sugar & Diabetes | Emerging | |
| rs2943634 | IRS1 | Intergenic variant near IRS1 at 2q36.3 associated with ischemic stroke risk, ... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs29941 | KCTD15 | GWAS obesity locus near KCTD15 — modulates adipogenesis through AP-2 transcri... | Appetite & Obesity | Moderate | |
| rs369296618 | MMAB | Nonsense variant in MMAB creating a premature stop codon (Q234*) that impairs... | Vitamins & Nutrient Absorption | Established | |
| rs137853334 | HNF4A HNF4A MODY1 Variant | Pathogenic nonsense variant in HNF4A causing MODY1 — a progressive, autosomal... | Blood Sugar & Diabetes | Established | |
| rs476828 | MC4R MC4R-region BMI variant | Intergenic variant in the MC4R regulatory haplotype block, tagging the same a... | Appetite & Obesity | Strong | |
| rs6259 | SHBG Asp356Asn | Missense variant in SHBG exon 8 (p.Asp356Asn, historically Asp327Asn in matur... | Reproductive Hormones | Moderate | |
| rs6837293 | PRKG2 | Intronic variant in PRKG2 (cGMP-dependent protein kinase II); the T allele wa... | Uric Acid & Kidney Function | Emerging | |
| rs267606993 | PYGM PYGM Met1Val (start-loss) | Pathogenic start-codon variant in muscle glycogen phosphorylase; homozygous o... | Metabolic Enzymes & Rare Disorders | Established | |
| rs3832024 | FMO3 FMO3 c.591_592del | A 2-bp frameshift deletion in FMO3 that creates a premature stop codon at pos... | Vitamins & Nutrient Absorption | Established | |
| rs4788102 | SH2B1 SH2B1/APOBR locus variant | Intronic variant at the SH2B1 locus on chromosome 16p11.2 — a key adaptor pro... | Appetite & Obesity | Strong | |
| rs1495377 | TSPAN8 | Intronic variant in TSPAN8 (Tetraspanin 8) associated with reduced insulin se... | Blood Sugar & Diabetes | Strong | |
| rs489693 | MC4R MC4R AIWG variant | Intergenic variant near MC4R with genome-wide significant association with an... | Appetite & Obesity | Strong | |
| rs1800592 | UCP1 A-3826G | Promoter variant reducing UCP1 expression in brown adipose tissue, impairing ... | Fat Storage & Energy | Moderate | |
| rs28933978 | OTC R141Q (Arg141Gln) | The most common OTC point mutation, abolishing ornithine transcarbamylase enz... | Metabolic Enzymes & Rare Disorders | Established | |
| rs28936415 | PMM2 R141H | The most common pathogenic PMM2 variant, causing phosphomannomutase 2 deficie... | Metabolic Enzymes & Rare Disorders | Established | |
| rs397507173 | BTD | Rare missense variant in the biotinidase enzyme (p.Pro167Ser); a likely patho... | Vitamins & Nutrient Absorption | Established | |
| rs2197076 | FABP1 | Intronic FABP1 variant associated with type 2 diabetes risk and insulin resis... | Triglycerides & Fatty Acids | Moderate | |
| rs367543005 | ASL p.Gln354Ter (Q354X) | Nonsense mutation in argininosuccinate lyase introducing a premature stop cod... | Metabolic Enzymes & Rare Disorders | Established | |
| rs571312 | MC4R MC4R Regulatory Variant (Appetite Signaling) | Regulatory variant upstream of MC4R associated with increased caloric intake,... | Appetite & Obesity | Strong | |
| rs182052 | ADIPOQ ADIPOQ promoter -10066A>G | Intronic/promoter-region ADIPOQ variant where the A allele reduces circulatin... | Fat Storage & Energy | Strong | |
| rs370793608 | ALDOB ALDOB Y204X | Nonsense variant in the aldolase B gene creating a premature stop codon at po... | Metabolic Enzymes & Rare Disorders | Established | |
| rs398123138 | BTD | Pathogenic 5-bp frameshift deletion in the biotinidase enzyme gene, eliminati... | Vitamins & Nutrient Absorption | Established | |
| 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 | |
| rs1800961 | HNF4A Thr130Ile | Missense variant in HNF4A causing hepatocyte-specific loss of transcriptional... | Blood Sugar & Diabetes | Moderate | |
| rs2297508 | SREBF1 SREBF1 G952G | SREBF1 3' UTR variant that subtly impairs SREBP-1c function, increasing risk ... | Fat Storage & Energy | Moderate | |
| rs1801278 | IRS1 Gly972Arg (G972R) | Missense variant in insulin receptor substrate 1 that impairs tyrosine phosph... | Blood Sugar & Diabetes | Strong | |
| rs72552272 | SLC7A7 L334R | Pathogenic missense in the y+LAT1 cationic amino acid transporter causing lys... | Metabolic Enzymes & Rare Disorders | Established | |
| rs72552297 | OTC Asn10fs (c.29_32del) | Frameshift deletion in the OTC gene that eliminates ornithine transcarbamylas... | Metabolic Enzymes & Rare Disorders | Established | |
| rs74315294 | CPT2 p.Ser113Leu (S113L) | Missense variant in CPT2 that destabilizes the carnitine palmitoyltransferase... | Metabolic Enzymes & Rare Disorders | Established | |
| rs2291725 | GIP Ser103Gly | Missense variant in the GIP incretin hormone that changes its bioactivity and... | Hormones & Sleep | Moderate | |
| rs4235308 | PPARGC1A | Intronic variant in the PGC-1alpha gene linked to population-specific type 2 ... | Fitness & Body | Emerging | |
| rs80338701 | PMM2 F119L | Second most common pathogenic PMM2 allele (p.Phe119Leu); in compound heterozy... | Metabolic Enzymes & Rare Disorders | Established | |
| rs2920502 | PPARG PPARG rs2920502 | Intronic PPARG variant associated with body fat percentage, impaired glucose ... | Fat Storage & Energy | Moderate | |
| rs7647305 | ETV5 | GWAS obesity locus near ETV5 — affects hypothalamic appetite regulation and f... | Appetite & Obesity | Moderate | |
| rs2233580 | PAX4 Arg192His | Missense variant that impairs PAX4's ability to repress insulin and glucagon ... | Blood Sugar & Diabetes | Strong | |
| 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 | |
| rs62623713 | SYPL2 E99G | Low-frequency missense variant in SYPL2 associated with morbid obesity suscep... | Fitness & Body | Emerging | |
| rs2295490 | TRIB3 Q84R | TRIB3 pseudokinase missense variant that increases Akt inhibition, impairing ... | Blood Sugar & Diabetes | Strong | |
| rs3745012 | LPIN2 LPIN2 3'UTR variant | 3' UTR regulatory variant in LPIN2 (lipin 2) that alters fat distribution and... | Fat Storage & Energy | Moderate | |
| rs3774261 | ADIPOQ ADIPOQ rs3774261 | Intronic ADIPOQ variant that reduces circulating adiponectin levels in G alle... | Fat Storage & Energy | Moderate | |
| rs9939609 | FTO Intron 1 T>A | The most strongly replicated obesity-associated variant, affecting body weigh... | Appetite & Obesity | Established | |
| rs3816873 | MTTP MTTP I128T | Missense variant in MTTP (microsomal triglyceride transfer protein) at residu... | Fat Storage & Energy | Moderate | |
| rs7181866 | GABPB1 | Intronic variant in the mitochondrial biogenesis regulator NRF2, associated w... | Fitness & Body | Moderate | |
| rs2943641 | IRS1 Near-gene C>T | Regulates insulin signaling efficiency and cellular glucose uptake | Blood Sugar & Diabetes | Strong | |
| rs3487348 | PTPN1 PTPN1 LD Block Co-Variant | Intronic PTPN1 variant in the 100-kb haplotype block; T allele associated wit... | Blood Sugar & Diabetes | Moderate | |
| rs391300 | SRR SRR rs391300 | Intronic variant in serine racemase that alters D-serine production in pancre... | Blood Sugar & Diabetes | Moderate | |
| rs6809631 | PPARG | Intronic PPARG promoter tagSNP associated with modest reduction in type 2 dia... | Fat Storage & Energy | Emerging | |
| rs5085 | APOA2 APOA2 rs5085 | Intronic APOA2 tag SNP that captures the saturated fat-weight gain interactio... | Triglycerides & Fatty Acids | 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 | |
| rs5956 | CD36 | Synonymous coding variant in CD36 fatty acid translocase; the minor A allele ... | Triglycerides & Fatty Acids | Emerging | |
| rs492594 | G6PC2 Val219Leu | Coding variant in the islet glucose-6-phosphatase that fine-tunes the fasting... | Blood Sugar & Diabetes | Moderate | |
| rs7649970 | PPARG PPARG C-689T | PPARG PPARγ2 P2 promoter variant that reduces basal promoter activity, elevat... | Fat Storage & Energy | Moderate | |
| rs5015480 | HHEX HHEX/IDE locus variant | Regulatory variant near HHEX and IDE linked to impaired beta-cell development... | Blood Sugar & Diabetes | Established | |
| rs767870 | ADIPOR2 ADIPOR2 intron 6 variant | Intronic variant in ADIPOR2 (adiponectin receptor 2) associated with reduced ... | Fat Storage & Energy | Moderate | |
| rs5210 | KCNJ11 KCNJ11 Kir6.2 Co-Variant | A regulatory 3' UTR variant in KCNJ11 that modulates KATP channel expression ... | Blood Sugar & Diabetes | Moderate | |
| rs5219 | KCNJ11 E23K | Controls the pancreatic beta-cell potassium channel that regulates insulin se... | Blood Sugar & Diabetes | Strong | |
| rs9817428 | PPARG PPARG promoter tagSNP | Intronic PPARG tagSNP with cross-ethnic replication for type 2 diabetes risk ... | Fat Storage & Energy | Emerging | |
| rs564398 | CDKN2B-AS1 | Secondary T2D risk variant at the 9p21 CDKN2A/B locus within ANRIL (CDKN2B-AS... | Blood Sugar & Diabetes | Moderate | |
| rs6017340 | HNF4A HNF4A Regulatory Variant | Intronic HNF4A tag SNP associated with altered bile acid synthesis regulation... | Blood Sugar & Diabetes | Emerging |