Tag
Micronutrients
91 genetic variants with this tag.
| RSID | Gene | Description | Category | ||
|---|---|---|---|---|---|
| rs10063949 | SLC23A1 SLC23A1 variant | Intronic variant in the intestinal and renal vitamin C transporter gene (SVCT... | Vitamins & Nutrient Absorption | Moderate | |
| rs10745742 | AMDHD1 | Intronic variant in the histidine-catabolism gene AMDHD1 that influences circ... | Metabolic Enzymes & Rare Disorders | Strong | |
| rs10766197 | CYP2R1 | Reduces CYP2R1 promoter activity and hepatic 25-hydroxylase expression, lower... | Vitamin D Metabolism | Strong | |
| rs11277 | SLC30A1 ZnT1 variant | 3'UTR regulatory variant in the primary intestinal zinc efflux transporter, w... | Iron & Mineral Transport | Emerging | |
| rs104893665 | SPR Arg150Gly | Pathogenic missense variant in sepiapterin reductase that abolishes BH4 biosy... | Vitamins & Nutrient Absorption | Established | |
| rs10832310 | CYP2R1 | Intronic tag SNP at the CYP2R1/PDE3B locus on chromosome 11 that marks a hapl... | Vitamin D Metabolism | Strong | |
| rs1165196 | SLC17A1 SLC17A1 T269I (NPT1) | Missense variant in SLC17A1 (NPT1) encoding a Thr269Ile substitution; the G a... | Uric Acid & Kidney Function | Moderate | |
| rs121434287 | SLC39A4 SLC39A4 zinc transporter variant | Pathogenic missense variant in the intestinal zinc transporter ZIP4, causing ... | Iron & Mineral Transport | Established | |
| rs1148259 | ANKRD30A | Synonymous variant in the 3′ UTR of ANKRD30A associated with altered circulat... | Metabolic Enzymes & Rare Disorders | Emerging | |
| rs1155563 | GC | Third independent intronic tag SNP in the vitamin D binding protein gene, inf... | Vitamin D Metabolism | Strong | |
| rs1165205 | SLC17A3 SLC17A3 variant (NPT4) | Intronic variant in SLC17A3, encoding the renal apical urate efflux transport... | Uric Acid & Kidney Function | Moderate | |
| rs121434288 | SLC39A4 SLC39A4 zinc transporter variant | Pathogenic missense variant in the ZIP4 intestinal zinc transporter causing h... | Iron & Mineral Transport | Established | |
| rs11950646 | SLC23A1 | Intronic variant in the intestinal and renal vitamin C transporter gene (SVCT... | Vitamins & Nutrient Absorption | Moderate | |
| rs121434289 | SLC39A4 Gly374Arg | Missense variant in ZIP4 zinc transporter causing total loss of intestinal zi... | Iron & Mineral Transport | Established | |
| rs1183201 | SLC17A1 | Intronic variant in SLC17A1 (NPT1), the renal apical urate efflux transporter... | Uric Acid & Kidney Function | Strong | |
| rs121434290 | SLC39A4 SLC39A4 p.Asn106Lys | Pathogenic missense variant in the ZIP4 intestinal zinc transporter; homozygo... | Iron & Mineral Transport | Established | |
| rs121917746 | SPR Q119X | Nonsense variant in sepiapterin reductase that abolishes BH4 biosynthesis, ca... | Vitamins & Nutrient Absorption | Established | |
| rs121434291 | SLC39A4 SLC39A4 zinc transporter variant | Pathogenic missense variant in the ZIP4 intestinal zinc transporter causing h... | Iron & Mineral Transport | Established | |
| rs121917747 | SPR | Nonsense variant in sepiapterin reductase creating a premature stop codon (p.... | Vitamins & Nutrient Absorption | Established | |
| rs121434280 | ACADM ACADM Y67H | Pathogenic missense variant in the MCAD enzyme causing a temperature-sensitiv... | Metabolic Enzymes & Rare Disorders | Strong | |
| rs121434292 | SLC39A4 Arg95Cys | Pathogenic missense variant in ZIP4, the primary intestinal zinc transporter,... | Iron & Mineral Transport | Established | |
| rs2060793 | CYP2R1 | Upstream regulatory variant in CYP2R1 that reduces hepatic 25-hydroxylase exp... | Vitamin D Metabolism | Strong | |
| rs121434293 | SLC39A4 SLC39A4 Gln278His | Pathogenic missense variant in the ZIP4 intestinal zinc transporter causing a... | Iron & Mineral Transport | Established | |
| rs12734494 | SLC30A1 | Intergenic variant near SLC30A1 (ZnT1), the primary basolateral zinc exporter... | Vitamins & Nutrient Absorption | Emerging | |
| rs1279683 | SLC23A2 | Intronic variant in the SVCT2 vitamin C transporter — G allele associated wit... | Vitamins & Nutrient Absorption | Moderate | |
| rs225011 | DIO2 | Intronic DIO2 variant nominally associated with Graves' disease susceptibilit... | Vitamin D Metabolism | Emerging | |
| rs121434369 | GCDH R402W (Arg402Trp) | Most common European allele for glutaric acidemia type 1; complete loss of GC... | Metabolic Enzymes & Rare Disorders | Established | |
| rs225015 | DIO2 DIO2 rs225015 | 3' UTR regulatory variant in DIO2 that may alter local thyroid hormone availa... | Vitamin D Metabolism | Moderate | |
| rs1151996 | PPARG PPARG rs1151996 | Intronic PPARG variant significantly associated with circulating vitamin D le... | Fat Storage & Energy | Moderate | |
| rs12144344 | ST6GALNAC3 | Intronic variant in sialyltransferase ST6GALNAC3 associated with higher circu... | Metabolic Enzymes & Rare Disorders | Emerging | |
| rs12272669 | UNKNOWN | Intergenic variant on chromosome 11q13.4 associated with circulating vitamin ... | Appetite & Obesity | Emerging | |
| rs145946881 | MCM6 -14010G>C | African lactase persistence variant — MCM6 enhancer SNP that controls LCT exp... | Vitamins & Nutrient Absorption | Strong | |
| rs1532423 | CA1 | Intronic variant in the carbonic anhydrase 1 gene cluster on chromosome 8 ass... | Uric Acid & Kidney Function | Moderate | |
| rs1800730 | HFE S65C | Third HFE variant associated with hemochromatosis; mildly impairs iron regula... | Iron & Mineral Transport | Moderate | |
| rs2282679 | GC | Intronic GWAS tag variant in the vitamin D binding protein gene, the stronges... | Vitamin D Metabolism | Established | |
| rs121908677 | SLC7A7 SLC7A7 p.Gly54Val | Pathogenic missense variant in the y+LAT1 cationic amino acid transporter; ho... | Metabolic Enzymes & Rare Disorders | Established | |
| rs148234606 | SLC52A2 Leu339Pro | Pathogenic missense variant in the riboflavin transporter RFVT2 that abolishe... | Vitamins & Nutrient Absorption | Established | |
| rs200482978 | SLC39A4 | Pathogenic nonsense variant in the intestinal zinc transporter ZIP4, creating... | Iron & Mineral Transport | Established | |
| rs182506368 | SLC39A4 SLC39A4 p.Ala99Thr | Pathogenic missense variant in the ZIP4 intestinal zinc transporter causing h... | Vitamins & Nutrient Absorption | Established | |
| rs2075674 | TFR2 TFR2 Ala617 variant | Synonymous coding variant in transferrin receptor 2 with potential splice-mod... | Iron & Mineral Transport | Emerging | |
| rs1871534 | SLC39A4 Leu372Val | Common missense variant in the primary intestinal zinc transporter ZIP4; the ... | Vitamins & Nutrient Absorption | Strong | |
| rs4752 | GC GC rs4752 | Synonymous variant in vitamin D binding protein that tags distinct GC haploty... | Vitamin D Metabolism | Moderate | |
| rs142967670 | GCDH R88C | Pathogenic missense variant in glutaryl-CoA dehydrogenase; homozygosity cause... | Metabolic Enzymes & Rare Disorders | Established | |
| rs2120019 | PPCDC | Intronic variant in PPCDC associated with lower circulating serum zinc levels... | Vitamins & Nutrient Absorption | Moderate | |
| rs228921 | TMPRSS6 TMPRSS6 iron regulation variant | Upstream regulatory variant near TMPRSS6 that independently lowers hemoglobin... | Iron & Mineral Transport | Strong | |
| rs7041 | GC Asp432Glu | Vitamin D binding protein variant that determines VDBP isoform, affecting vit... | Vitamin D Metabolism | Strong | |
| rs174548 | FADS1 | Intronic regulatory variant in FADS1 that reduces delta-5 desaturase expressi... | Triglycerides & Fatty Acids | Strong | |
| rs2235321 | TMPRSS6 TMPRSS6 synonymous variant (hepcidin modulator) | Synonymous coding variant in TMPRSS6 associated with hepcidin levels and iron... | Vitamins & Nutrient Absorption | Moderate | |
| rs2413450 | TMPRSS6 TMPRSS6 iron regulation variant | Intronic TMPRSS6 variant associated with lower MCV, MCH, and hemoglobin level... | Iron & Mineral Transport | Strong | |
| rs705117 | GC | Intronic GC variant independently associated with vitamin D binding protein (... | Vitamin D Metabolism | Strong | |
| rs3738198 | SLC30A1 ZnT1 variant | Intronic variant in the ZnT1 zinc efflux transporter gene; the minor C allele... | Iron & Mineral Transport | Emerging | |
| rs7936142 | CYP2R1 CYP2R1 rs7936142 | Intronic variant in the primary hepatic vitamin D 25-hydroxylase gene associa... | Vitamin D Metabolism | Moderate | |
| rs174561 | FADS1 | Intronic variant in the FADS1 gene cluster that tags a haplotype block contro... | Triglycerides & Fatty Acids | Strong | |
| rs387907018 | TMPRSS6 Matriptase-2 E522K | Rare pathogenic TMPRSS6 missense in the LDLRA2 domain that impairs hemojuveli... | Iron & Mineral Transport | Strong | |
| rs2413775 | SLC28A2 | Promoter variant that increases SLC28A2/CNT2 transcription via enhanced HNF1 ... | Vitamins & Nutrient Absorption | Emerging | |
| rs4519796 | SLC2A9 SLC2A9 rs4519796 | Intronic SLC2A9 tag variant tracking the GLUT9 urate-reabsorption haplotype; ... | Uric Acid & Kidney Function | Emerging | |
| rs4820268 | TMPRSS6 TMPRSS6 D512E | TMPRSS6 missense variant affecting matriptase-2 activity; A allele (Asp512Glu... | Iron & Mineral Transport | Strong | |
| rs174572 | FADS2 | Intronic variant in FADS2 that reduces delta-6 desaturase activity, impairing... | Triglycerides & Fatty Acids | Strong | |
| rs28941784 | MMAB Arg186Trp (R186W) | Missense variant eliminating MMAB adenosylcobalamin synthase activity; the mo... | Vitamins & Nutrient Absorption | Established | |
| rs4580649 | SLC2A9 SLC2A9 rs4580649 | Intronic variant in the major renal urate transporter SLC2A9 (GLUT9); the A a... | Uric Acid & Kidney Function | Moderate | |
| rs5756504 | TMPRSS6 TMPRSS6 variant | Intronic TMPRSS6 variant associated with hemoglobin levels and erythrocyte pa... | Iron & Mineral Transport | Moderate | |
| rs842999 | GC | Intronic GC variant tagging a haplotype associated with lower circulating 25-... | Vitamin D Metabolism | Moderate | |
| rs2034650 | IVD | Intronic regulatory variant in IVD (isovaleryl-CoA dehydrogenase) associated ... | Metabolic Enzymes & Rare Disorders | Emerging | |
| rs5756506 | TMPRSS6 | Intronic TMPRSS6 variant associated with hemoglobin and hematocrit levels, in... | Iron & Mineral Transport | Emerging | |
| rs33972313 | SLC23A1 Val264Met | Primary intestinal and renal vitamin C transporter — variant reduces ascorbat... | Vitamins & Nutrient Absorption | Strong | |
| rs7385804 | TFR2 | Intronic variant in transferrin receptor 2 that tags altered TFR2 expression ... | Iron & Mineral Transport | Strong | |
| rs17606561 | ELOVL2 | 3'-UTR variant in ELOVL2 associated with altered EPA-to-DHA conversion; A all... | Triglycerides & Fatty Acids | Moderate | |
| rs3877899 | SELENOP Ala234Thr | Missense variant in selenoprotein P that alters selenium transport capacity; ... | Vitamins & Nutrient Absorption | Moderate | |
| rs397507172 | BTD | Rare missense variant near the BTD active site (p.Val89Gly) that likely reduc... | Vitamins & Nutrient Absorption | Emerging | |
| 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 | |
| rs397507174 | BTD BTD Tyr190Cys | Pathogenic missense variant in biotinidase that abolishes biotin recycling; h... | Vitamins & Nutrient Absorption | Established | |
| rs7435196 | SLC2A9 | Intronic SLC2A9 variant located within the GLUT9 renal urate transporter gene... | Uric Acid & Kidney Function | Emerging | |
| rs397514538 | SLC52A2 | Pathogenic missense variant in riboflavin transporter RFVT2 (p.Leu123Pro) cau... | Vitamins & Nutrient Absorption | Established | |
| rs7660895 | SLC2A9 | Intronic variant in the major renal urate transporter GLUT9; the G allele red... | Uric Acid & Kidney Function | Strong | |
| rs398123138 | BTD | Pathogenic 5-bp frameshift deletion in the biotinidase enzyme gene, eliminati... | Vitamins & Nutrient Absorption | Established | |
| rs41380347 | MCM6 G-13915T | East African lactase persistence allele — MCM6 enhancer SNP that independentl... | Vitamins & Nutrient Absorption | Strong | |
| rs4434553 | TFR2 TFR2 upstream variant | Regulatory variant 2 kb upstream of TFR2 that modulates hepcidin production a... | Vitamins & Nutrient Absorption | Emerging | |
| 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 | |
| rs2727270 | FADS2 | Intronic regulatory variant in FADS2 that tags a 10-SNP haplotype reducing ba... | Triglycerides & Fatty Acids | Moderate | |
| rs5753231 | TCN2 TCN2 2KB Upstream Variant | Promoter-proximal upstream variant in TCN2 that increases transcobalamin II p... | Vitamins & Nutrient Absorption | Emerging | |
| rs72552297 | OTC Asn10fs (c.29_32del) | Frameshift deletion in the OTC gene that eliminates ornithine transcarbamylas... | Metabolic Enzymes & Rare Disorders | Established | |
| rs8018720 | SEC23A | Missense variant in the COPII vesicle coat protein SEC23A, associated with ci... | Metabolic Enzymes & Rare Disorders | Emerging | |
| rs2854747 | IGFBP3 | Intronic variant in IGFBP3 — the gene encoding the main carrier protein for I... | Fat Storage & Energy | Moderate | |
| rs6053005 | SLC23A2 | Intronic variant in the SVCT2 tissue vitamin C transporter — associated with ... | Vitamins & Nutrient Absorption | Moderate | |
| rs80338701 | PMM2 F119L | Second most common pathogenic PMM2 allele (p.Phe119Leu); in compound heterozy... | Metabolic Enzymes & Rare Disorders | Established | |
| rs6133175 | SLC23A2 | Intronic variant in the tissue vitamin C transporter SVCT2 — GG homozygotes c... | Vitamins & Nutrient Absorption | Moderate | |
| rs6596471 | SLC23A1 SLC23A1 variant | Intronic variant in the intestinal and renal vitamin C transporter gene (SVCT... | Vitamins & Nutrient Absorption | Moderate | |
| rs6596473 | SLC23A1 SLC23A1 variant | Intronic variant in the intestinal and renal vitamin C transporter gene (SVCT... | Vitamins & Nutrient Absorption | Emerging | |
| rs99780 | FADS2 | Intronic variant in the FADS1-FADS2 cluster influencing delta-6 desaturase ac... | Triglycerides & Fatty Acids | Moderate |