Tag
Oxidative Stress
63 genetic variants with this tag.
| RSID | Gene | Description | Category | ||
|---|---|---|---|---|---|
| rs1001179 | CAT -262C>T | Catalase promoter variant affecting hydrogen peroxide clearance and antioxida... | Methylation & Detox | Strong | |
| rs1049255 | CYBA CYBA 3'UTR A640G | 3'UTR variant in the NADPH oxidase p22-phox subunit affecting superoxide gene... | Vascular Inflammation & Remodeling | Moderate | |
| rs11235972 | UCP3 | Intronic UCP3 variant associated with skeletal muscle fat oxidation capacity,... | Liver Fat | Moderate | |
| rs1021737 | CTH CTH Ser403Ile | Missense variant in CTH (cystathionine gamma-lyase) that impairs transsulfura... | Blood Pressure & Hypertension | Moderate | |
| rs1136410 | PARP1 Val762Ala | Missense variant in the PARP1 catalytic domain that reduces enzymatic activit... | Longevity & Aging | Strong | |
| rs1050450 | GPX1 Pro198Leu | Selenium-dependent antioxidant enzyme that neutralizes hydrogen peroxide; the... | Methylation & Detox | Strong | |
| rs11555236 | SIRT3 | Intronic regulatory variant near the SIRT3 VNTR enhancer — the A allele incre... | Longevity & Aging | Moderate | |
| rs12206094 | FOXO3 | Functional FOXO3 intronic variant with allele-specific CTCF binding and IGF-1... | Longevity & Aging | Strong | |
| rs12212067 | FOXO3 | Intronic FOXO3 variant whose minor G allele creates an MZF1 transcription fac... | Longevity & Aging | Strong | |
| rs12704795 | PON2 PON2 intron 1 variant | Intronic PON2 haplotype tag; the A allele is associated with reduced intracel... | Vascular Inflammation & Remodeling | Moderate | |
| rs1154404 | ADH5 ADH5 Asthma Risk Haplotype Variant | Intronic variant in ADH5 (GSNOR) in near-complete LD (r²=0.99) with adjacent ... | Allergy & Atopic Disease | Moderate | |
| rs13181 | ERCC2 Lys751Gln | Missense variant in the XPD helicase that reduces nucleotide excision repair ... | Longevity & Aging | Strong | |
| rs1805007 | MC1R R151C | Strongest "R" allele in the melanocortin-1 receptor, shifting pigment from ph... | Skin & Eyes | Established | |
| rs13217795 | FOXO3 | Original 2008 Willcox longevity discovery variant; C allele tags the protecti... | Longevity & Aging | Strong | |
| rs2075674 | TFR2 TFR2 Ala617 variant | Synonymous coding variant in transferrin receptor 2 with potential splice-mod... | Iron & Mineral Transport | Emerging | |
| rs2278651 | SLC30A1 ZnT1 variant | Intronic variant in SLC30A1 (ZnT1), the primary plasma-membrane zinc efflux t... | Iron & Mineral Transport | Emerging | |
| rs1138272 | GSTP1 Ala114Val | Second functional variant in glutathione S-transferase Pi 1, reducing enzyme ... | Methylation & Detox | Moderate | |
| rs11931074 | SNCA | SNCA 3′-region variant in the extended 3′ UTR that affects alpha-synuclein mR... | Neurology & Cognition | Strong | |
| rs2251780 | GSR | Intronic variant in the glutathione reductase gene affecting antioxidant defe... | Vitamins & Nutrient Absorption | Emerging | |
| rs1935949 | FOXO3 | Second independent FOXO3 longevity signal tagging a distinct intronic haploty... | Longevity & Aging | Moderate | |
| rs12598836 | HMOX2 | Intronic variant near heme oxygenase 2 (HMOX2) associated with migraine-with-... | Neurology & Cognition | Moderate | |
| rs1937 | TFAM S12T | Missense variant in the TFAM mitochondrial targeting sequence — the C allele ... | Longevity & Aging | Moderate | |
| rs482843 | CTH | Intronic CTH variant where GG homozygotes show significantly elevated preecla... | Blood Pressure & Hypertension | Moderate | |
| rs1800624 | AGER -374T/A | Promoter variant in the AGER gene that increases RAGE transcription approxima... | Hormones & Sleep | Moderate | |
| rs1800625 | AGER AGER -429T>C | Promoter variant at position -429 in the AGER gene that increases RAGE transc... | Hormones & Sleep | Moderate | |
| rs2153960 | FOXO3 | Intronic FOXO3 tag SNP whose A allele associates with higher circulating IGF-... | Longevity & Aging | Moderate | |
| rs3805435 | TNIP1 | Intronic variant in the GPX3/TNIP1 regulatory locus on chromosome 5; the C al... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs2253310 | FOXO3 | Intronic FOXO3 longevity variant; C allele (minor in East Asians) associated ... | Longevity & Aging | Moderate | |
| rs2237583 | PON1 PON1 intron variant | Intronic PON1 variant that modulates arylesterase activity of the HDL-bound a... | Vascular Inflammation & Remodeling | Moderate | |
| rs3877899 | SELENOP Ala234Thr | Missense variant in selenoprotein P that alters selenium transport capacity; ... | Vitamins & Nutrient Absorption | Moderate | |
| rs547025 | SIRT3 | Intronic variant in SIRT3 (the principal mitochondrial deacetylase) associate... | Endometriosis & Uterine Health | Moderate | |
| rs1695 | GSTP1 Ile105Val | Phase II detoxification enzyme that conjugates glutathione to carcinogens, dr... | Methylation & Detox | Strong | |
| rs17309872 | GSS | Downstream regulatory variant of glutathione synthetase (GSS) associated with... | Methylation & Detox | Moderate | |
| rs2228001 | XPC Lys939Gln | Missense variant in the DNA damage recognition gene XPC that reduces global-g... | Fitness & Body | Strong | |
| rs2070600 | AGER Gly82Ser | Missense variant in the AGER pattern-recognition receptor that reduces solubl... | Hormones & Sleep | Strong | |
| rs6757908 | EIF2AK3-AS1 | Rare intronic variant in EIF2AK3-AS1, an antisense long non-coding RNA that r... | Endometriosis & Uterine Health | Emerging | |
| rs2031920 | CYP2E1 *5B (RsaI) | Promoter variant increasing CYP2E1 inducibility, elevating oxidative stress f... | Pharmacogenomics | Moderate | |
| rs1800566 | NQO1 Pro187Ser (C609T) | Phase II detoxification enzyme that reduces quinones and recycles CoQ10 to it... | Methylation & Detox | Strong | |
| rs2764264 | FOXO3 | Intronic FOXO3 variant that disrupts an NKX3 transcription factor binding sit... | Longevity & Aging | Strong | |
| rs2779249 | NOS2 Promoter -1026C/A | Functional promoter variant that increases iNOS transcriptional activity up t... | Longevity & Aging | Moderate | |
| rs2802292 | FOXO3 | Longevity-associated intronic enhancer variant with 1.9-fold increased probab... | Longevity & Aging | Established | |
| rs4729189 | PON2 | Intronic PON2 variant associated with variation in serum paraoxonase activity... | Vascular Inflammation & Remodeling | Emerging | |
| rs705379 | PON1 PON1 promoter -108C>T | Promoter polymorphism that controls PON1 gene expression — the T allele (A on... | Vascular Inflammation & Remodeling | Strong | |
| rs854555 | PON1 PON1 3'UTR variant | Intronic/downstream PON1 haplotype-tagging variant associated with PON1 activ... | Vascular Inflammation & Remodeling | Emerging | |
| rs3758391 | SIRT1 | Promoter-region variant in SIRT1 affecting deacetylase expression; T allele e... | Longevity & Aging | Moderate | |
| rs854571 | PON1 PON1 -108C>T promoter variant | Promoter variant that controls PON1 transcription; the T allele reduces PON1 ... | Vascular Inflammation & Remodeling | Strong | |
| rs854572 | PON1 PON1 promoter -909G>C | Promoter polymorphism that modulates PON1 gene expression level — the G allel... | Vascular Inflammation & Remodeling | Moderate | |
| rs4946935 | FOXO3 | Functionally validated FOXO3 intronic variant that creates an SRF binding sit... | Longevity & Aging | Strong | |
| rs887829 | UGT1A1 UGT1A1*80 | Promoter variant in UGT1A1 that tags the *28 reduced-expression haplotype; T ... | Vascular Inflammation & Remodeling | Strong | |
| rs659366 | UCP2 | Promoter variant at position -866 of UCP2 that controls mitochondrial uncoupl... | Longevity & Aging | Moderate | |
| rs6721961 | NFE2L2 | Promoter variant reducing NRF2 transcriptional activity by >50%, impairing th... | Longevity & Aging | Moderate | |
| rs2583988 | SNCA | SNCA upstream regulatory variant (near gene-5) that is part of the 4-SNP SNCA... | Neurology & Cognition | Emerging | |
| rs2736990 | SNCA | Intronic SNCA variant (intron 4) associated with Parkinson's disease risk and... | Neurology & Cognition | Strong | |
| rs7895833 | SIRT1 A>G | Intronic variant in SIRT1 affecting NAD-dependent deacetylase expression and ... | Longevity & Aging | Moderate | |
| rs366631 | GSTM1 Tag SNP for gene deletion | Tag SNP proxy for GSTM1 gene deletion status — the most common pharmacogenomi... | Methylation & Detox | Strong | |
| rs4746 | GLO1 Glu111Ala | Missense variant in glyoxalase 1 reducing enzyme activity, allowing methylgly... | Hormones & Sleep | Moderate | |
| rs356182 | SNCA | Parkinson's disease GWAS risk variant affecting alpha-synuclein expression an... | Neurology & Cognition | Strong | |
| rs356219 | SNCA | SNCA 3′-region regulatory variant that upregulates alpha-synuclein expression... | Neurology & Cognition | Strong | |
| rs5030868 | G6PD G6PD Mediterranean | Severe Class II G6PD deficiency variant (c.563C>T, p.Ser188Phe) causing less ... | Blood Sugar & Diabetes | Established | |
| rs2851301 | ADH5 ADH5 Second NF-kB Site Variant | Upstream promoter variant in ADH5 at a potential NF-kB binding site; the mino... | Allergy & Atopic Disease | Emerging | |
| rs28730619 | ADH5 | Intronic variant in ADH5 (GSNOR) associated with elevated childhood asthma ri... | Allergy & Atopic Disease | Moderate | |
| rs4880 | SOD2 Val16Ala | Primary mitochondrial antioxidant enzyme - variant reduces superoxide detoxif... | Methylation & Detox | Strong | |
| rs76723693 | G6PD G6PD Nefza (c.968T>C) | Missense variant in glucose-6-phosphate dehydrogenase causing Class III G6PD ... | Blood Sugar & Diabetes | Strong |