Research
Tag

Pain Sensitivity

24 genetic variants with this tag.

RSID Gene Description Category
rs1003194 CALCA/CALCB Intergenic regulatory variant ~26 kb downstream of CALCB (calcitonin gene-rel... Neurology & Cognition Strong
rs10166942 TRPM8 Upstream regulatory variant of the cold-sensing TRPM8 channel that modulates ... Neurology & Cognition Strong
rs10405121 CACNA1A Common intronic variant in CACNA1A — the P/Q-type calcium channel gene mutate... Neurology & Cognition Strong
rs10456100 KCNK5 Intronic variant near KCNK5 that reduces TASK2 potassium channel expression a... Neurology & Cognition Strong
rs1800629 TNF -308 G>A Promoter variant increasing TNF-alpha production approximately 2-fold, associ... TNF, NF-kB & Inflammatory Cytokines Strong
rs142885915 NPSR1 NPSR1 Endometriosis Risk Variant An intronic insertion/deletion variant in the neuropeptide S receptor 1 gene ... Endometriosis & Uterine Health Moderate
rs16147 NPY C-399T Promoter variant in neuropeptide Y that modulates NPY expression under stress... Mood & Behavior Moderate
rs1805007 MC1R R151C Strongest "R" allele in the melanocortin-1 receptor, shifting pigment from ph... Skin & Eyes Established
rs12598836 HMOX2 Intronic variant near heme oxygenase 2 (HMOX2) associated with migraine-with-... Neurology & Cognition Moderate
rs1718119 P2RX7 Ala348Thr Gain-of-function variant in the P2X7 receptor that increases ATP-gated pore f... Neurology & Cognition Moderate
rs689466 PTGS2 A-1195G Promoter variant in the PTGS2/COX-2 gene that reduces baseline COX-2 expressi... IBD & Mucosal Immunity Moderate
rs2078371 TSPAN2 Regulatory variant in the TSPAN2/NGF locus on chromosome 1p13; the C allele i... Neurology & Cognition Strong
rs208294 P2RX7 His155Tyr Gain-of-function missense variant in the P2X7 ATP-gated receptor that increas... Neurology & Cognition Moderate
rs2274319 MEF2D Intronic variant in MEF2D encoding a key neuronal transcription factor that r... Neurology & Cognition Strong
rs306960 PTK2 Intronic variant in PTK2 (focal adhesion kinase) linked to restless legs synd... Neurology & Cognition Strong
rs3791033 KDM4A Intronic variant in KDM4A histone demethylase associated with problematic opi... Pharmacogenomics Moderate
rs3751143 P2RX7 Glu496Ala Loss-of-function variant in the P2X7 receptor that reduces inflammatory respo... Neurology & Cognition Strong
rs61759167 PRDM16 Intronic PRDM16 variant reaching genome-wide significance in the first motion... Neurology & Cognition Strong
rs58194899 EIPR1 Intronic variant in EIPR1 (endosomal trafficking protein) associated with pai... Pharmacogenomics Emerging
rs6746030 SCN9A R1150W Common variant in the Nav1.7 sodium channel affecting pain sensitivity and pa... Neurology & Cognition Strong
rs6777055 CACNA2D3 Intronic variant affecting thermal pain sensitivity and central pain signal t... Neurology & Cognition Moderate
rs7958311 P2RX7 Arg270His P2RX7 variant with a unique dual mechanism — gain-of-function in channel open... Neurology & Cognition Moderate
rs8007267 GCH1 Promoter variant affecting GTP cyclohydrolase 1 expression and pain sensitivi... Neurology & Cognition Strong
rs8065080 TRPV1 Ile585Val Capsaicin receptor variant affecting heat and pain sensitivity Neurology & Cognition Strong