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 |