Research
Tag

Pain Medication

26 genetic variants with this tag.

RSID Gene Description Category
rs10403955 CYP2B6 Intronic CYP2B6 haplotype-tagging variant associated with altered plasma conc... Pharmacogenomics Moderate
rs1057910 CYP2C9 *3 No-function CYP2C9 variant with major warfarin implications Pharmacogenomics Established
rs1058164 CYP2D6 Synonymous CYP2D6 variant that promotes exon 3 skipping, reducing functional ... Pharmacogenomics Moderate
rs1065852 CYP2D6 *10 Decreased function CYP2D6 variant common in Asian populations Pharmacogenomics Established
rs1080985 CYP2D6 *2A promoter CYP2D6 promoter variant (-1584C>G) that reduces enzyme expression; the C alle... Pharmacogenomics Strong
rs1113129 CYP2C8 Intronic tagging SNP for CYP2C8 haplotype C, a low-activity haplotype associa... Pharmacogenomics Moderate
rs16947 CYP2D6 *2 Common CYP2D6 variant defining the *2 allele; previously considered normal-fu... Pharmacogenomics Strong
rs17002852 CYP2D6 Synonymous CYP2D6 variant that causes allele dropout in standard CYP2D6*3 gen... Pharmacogenomics Moderate
rs1799853 CYP2C9 *2 Decreased function variant affecting warfarin, phenytoin, and NSAIDs Pharmacogenomics Established
rs1799971 OPRM1 A118G Mu-opioid receptor variant affecting opioid response, pain sensitivity, and p... Pharmacogenomics Strong
rs1934963 CYP2C9 Deep intronic CYP2C9 variant associated with altered drug response to sulfony... Pharmacogenomics Emerging
rs1934967 CYP2C9 Intronic CYP2C9 haplotype tag associated with altered warfarin sensitivity an... Pharmacogenomics Moderate
rs2246709 CYP3A4 Intronic CYP3A4 variant associated with altered drug clearance, affecting met... Pharmacogenomics Moderate
rs28371706 CYP2D6 *17 Decreased-function CYP2D6 allele common in African populations, reducing meta... Pharmacogenomics Established
rs28371725 CYP2D6 *41 Intronic splice variant causing decreased CYP2D6 enzyme activity through aber... Pharmacogenomics Established
rs28371733 CYP2D6 Rare CYP2D6 stop-gain variant (Glu418Ter) that eliminates enzyme activity, ca... Pharmacogenomics Established
rs28695233 CYP2D6 Deep intronic CYP2D6 variant in intron 2 that serves as a haplotype tag in sp... Pharmacogenomics Emerging
rs373489637 CYP2B6 V183G Near-complete loss-of-function CYP2B6 variant causing severely impaired metab... Pharmacogenomics Moderate
rs3745274 CYP2B6 516G>T Decreased-function variant affecting metabolism of efavirenz, methadone, bupr... Pharmacogenomics Established
rs3892097 CYP2D6 *4 CYP2D6 *4 splice-defect null allele — the most common loss-of-function CYP2D6... Pharmacogenomics Established
rs5030655 CYP2D6 *6 Frameshift deletion causing no enzyme function, defining poor metabolizer sta... Pharmacogenomics Established
rs58440431 CYP2D6 Intronic CYP2D6 variant tagging East Asian *10-lineage suballeles; the C alle... Pharmacogenomics Strong
rs640561 LRRIQ3 Intergenic variant near LRRIQ3 associated with problematic opioid prescriptio... Pharmacogenomics Emerging
rs67807361 CYP2C9 p.Leu19Ile Rare CYP2C9 N-terminal missense variant of uncertain functional significance ... Pharmacogenomics Emerging
rs71328650 CYP2D6 Intronic CYP2D6 haplotype tag variant (rs28371702 canonical form) associated ... Pharmacogenomics Emerging
rs72549354 CYP2D6 *20 Frameshift insertion creating a null CYP2D6 allele; carriers cannot metaboliz... Pharmacogenomics Established