CYP2W1
cytochrome P450 family 2 subfamily W member 1
Pharmacogene
Summary
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. [provided by RefSeq, Jul 2008]
Known Variants65 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1316523256 | 7:983,384 | A/C | missense variant | — |
| rs78873069 | 7:988,643 | G/A | missense variant | — |
| rs773499447 | 7:988,795 | G/C | missense variant | — |
| rs12701220 | 7:1,022,728 | T/C | regulatory region variant | — |
| rs751702883 | 7:1,022,905 | G/A | — | uncertain significance |
| rs779903612 | 7:1,022,924 | C/T | — | uncertain significance |
| rs531323748 | 7:1,022,936 | G/A | — | uncertain significance |
| rs777039804 | 7:1,022,971 | G/A | — | uncertain significance |
| rs371785180 | 7:1,022,996 | C/T | — | uncertain significance |
| rs764341789 | 7:1,023,017 | T/C | — | uncertain significance |
| rs369965540 | 7:1,024,063 | G/C | — | uncertain significance |
| rs373912411 | 7:1,024,081 | C/T | — | uncertain significance |
| rs370828705 | 7:1,024,096 | A/G | — | uncertain significance |
| rs770182157 | 7:1,024,142 | C/T | — | likely benign |
| rs756831513 | 7:1,024,199 | A/G | — | uncertain significance |
| rs748420181 | 7:1,024,588 | A/G | — | uncertain significance |
| rs772487691 | 7:1,024,589 | T/G | — | uncertain significance |
| rs148638638 | 7:1,024,591 | T/A | — | uncertain significance |
| rs577187426 | 7:1,024,607 | C/T | — | uncertain significance |
| rs766068674 | 7:1,024,613 | G/T | — | uncertain significance |
| rs745905774 | 7:1,024,660 | G/A | — | uncertain significance |
| rs780161898 | 7:1,024,804 | C/T | — | uncertain significance |
| rs566834079 | 7:1,024,832 | G/C | — | uncertain significance |
| rs3735684 | 7:1,024,855 | G/A | missense variant | — |
| rs768066698 | 7:1,024,856 | C/T | — | uncertain significance |
| rs766555022 | 7:1,024,870 | C/T | — | uncertain significance |
| rs143596553 | 7:1,024,913 | G/C | — | uncertain significance |
| rs2483393094 | 7:1,026,264 | T/C | — | uncertain significance |
| rs565794893 | 7:1,026,269 | G/A | — | likely benign |
| rs764070881 | 7:1,026,275 | C/G | — | uncertain significance |
| rs148926756 | 7:1,026,283 | C/T | — | likely benign |
| rs1031091197 | 7:1,026,305 | C/T | — | uncertain significance |
| rs370589869 | 7:1,026,332 | G/A | — | uncertain significance |
| rs188617371 | 7:1,026,335 | C/T | — | uncertain significance |
| rs2128123786 | 7:1,026,359 | G/A | — | uncertain significance |
| rs78447922 | 7:1,026,365 | C/T | — | uncertain significance |
| rs746365436 | 7:1,026,366 | G/A | — | uncertain significance |
| rs749701988 | 7:1,026,371 | C/T | — | uncertain significance |
| rs61733260 | 7:1,026,385 | G/A | — | benign |
| rs763439785 | 7:1,026,395 | G/A | — | uncertain significance |
| rs780562848 | 7:1,026,421 | C/G | — | uncertain significance |
| rs749247516 | 7:1,026,759 | G/T | — | uncertain significance |
| rs536373592 | 7:1,026,774 | C/A | — | likely benign |
| rs186092597 | 7:1,026,870 | C/T | — | uncertain significance |
| rs763609907 | 7:1,026,876 | T/G | — | uncertain significance |
| rs745500143 | 7:1,026,988 | G/A | — | uncertain significance |
| rs149240463 | 7:1,027,007 | G/A | — | benign |
| rs200372185 | 7:1,027,033 | C/T | — | uncertain significance |
| rs755676275 | 7:1,027,034 | G/A | — | likely benign |
| rs1048949977 | 7:1,027,072 | G/A | — | uncertain significance |
| rs1848450854 | 7:1,027,075 | C/T | — | uncertain significance |
| rs752143691 | 7:1,027,100 | C/G | — | uncertain significance |
| rs1246200217 | 7:1,027,115 | T/C | — | uncertain significance |
| rs753528839 | 7:1,027,120 | C/T | — | uncertain significance |
| rs774470425 | 7:1,027,986 | A/G | — | uncertain significance |
| rs376135915 | 7:1,028,006 | G/A | — | uncertain significance |
| rs772261904 | 7:1,028,028 | G/C | — | uncertain significance |
| rs2483411709 | 7:1,028,049 | C/G | — | uncertain significance |
| rs778855184 | 7:1,028,295 | G/A | — | uncertain significance |
| rs776155897 | 7:1,028,348 | C/T | — | uncertain significance |
| rs752623475 | 7:1,028,375 | C/G | — | uncertain significance |
| rs376719334 | 7:1,028,438 | T/C | — | uncertain significance |
| rs3808348 | 7:1,028,448 | C/T | missense variant | — |
| rs12701278 | 7:1,029,549 | T/G | — | — |
| rs9769088 | 7:1,029,585 | T/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.