Research
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