Tag
Caffeine
9 genetic variants with this tag.
| RSID | Gene | Description | Category | ||
|---|---|---|---|---|---|
| rs2470890 | CYP1A2 Asn516= (exon 7) | Synonymous variant in CYP1A2 exon 7 in linkage disequilibrium with the *1F hi... | Cancer Risk | Strong | |
| rs2066853 | AHR Arg554Lys | Aryl hydrocarbon receptor variant in the transactivation domain that alters A... | Hormones & Sleep | Moderate | |
| rs2069526 | CYP1A2 -739T>G | Intronic CYP1A2 variant near the 5' end; G allele is associated with altered ... | Pharmacogenomics | Emerging | |
| rs4410790 | AHR | Regulatory variant 54 kb upstream of the aryl hydrocarbon receptor gene; the ... | Hormones & Sleep | Strong | |
| rs5751876 | ADORA2A 1976T>C | Adenosine A2A receptor variant that determines individual sensitivity to caff... | Hormones & Sleep | Strong | |
| rs72547511 | CYP1A2 CYP1A2*15 (Pro42Arg) | Rare CYP1A2 missense variant at the critical Pro42 position; nearly abolishes... | Pharmacogenomics | Moderate | |
| rs72547515 | CYP1A2 *16 (Arg377Gln) | Nearly-inactive CYP1A2 missense variant — carriers have severely impaired met... | Pharmacogenomics | Moderate | |
| rs72547516 | CYP1A2 Ile386Val | Rare CYP1A2 missense variant (Ile386Val) associated with potentially reduced ... | Pharmacogenomics | Emerging | |
| rs72547517 | CYP1A2 *8 | CYP1A2*8 — near-complete loss-of-function missense variant causing severely r... | Pharmacogenomics | Strong |