CCDC33
coiled-coil domain containing 33
Summary
Predicted to be active in peroxisome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants72 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs189088694 | 15:74,536,356 | G/A | — | likely benign |
| rs1433926647 | 15:74,536,374 | C/A | — | uncertain significance |
| rs201484902 | 15:74,536,403 | G/C | — | likely benign |
| rs201658615 | 15:74,536,467 | G/A | — | uncertain significance |
| rs375633934 | 15:74,536,471 | C/T | — | uncertain significance |
| rs79782206 | 15:74,542,912 | C/T | regulatory region variant | — |
| rs9783698 | 15:74,548,773 | G/T | — | — |
| rs117149087 | 15:74,549,076 | T/C | intron variant | — |
| rs4886593 | 15:74,558,078 | T/A | regulatory region variant | — |
| rs2548163791 | 15:74,560,699 | A/G | — | uncertain significance |
| rs572128186 | 15:74,560,728 | T/A | — | uncertain significance |
| rs567109737 | 15:74,560,737 | A/G | — | likely benign |
| rs777988742 | 15:74,560,740 | G/A | — | uncertain significance |
| rs2548164209 | 15:74,560,773 | A/G | — | uncertain significance |
| rs373542701 | 15:74,564,107 | C/T | — | uncertain significance |
| rs376212982 | 15:74,565,112 | G/T | — | uncertain significance |
| rs370347829 | 15:74,565,116 | A/G | — | uncertain significance |
| rs2076356278 | 15:74,565,179 | C/T | — | likely benign |
| rs1011295381 | 15:74,565,183 | C/T | — | uncertain significance |
| rs370366309 | 15:74,565,209 | G/A | — | likely benign |
| rs769976545 | 15:74,572,320 | G/A | — | uncertain significance |
| rs758671441 | 15:74,573,030 | C/T | — | uncertain significance |
| rs115546722 | 15:74,573,128 | C/T | — | uncertain significance |
| rs1178136019 | 15:74,574,123 | C/T | — | uncertain significance |
| rs374865411 | 15:74,574,135 | C/T | — | uncertain significance |
| rs373900085 | 15:74,574,158 | G/A | — | uncertain significance |
| rs138672210 | 15:74,580,598 | A/G | intron variant | — |
| rs1306973922 | 15:74,588,114 | C/T | — | uncertain significance |
| rs1243781003 | 15:74,588,158 | C/G | — | uncertain significance |
| rs1343975174 | 15:74,588,202 | C/A | — | uncertain significance |
| rs1399893506 | 15:74,588,203 | A/G | — | uncertain significance |
| rs2548228743 | 15:74,588,253 | G/T | — | uncertain significance |
| rs370287933 | 15:74,588,282 | A/G | — | likely benign |
| rs11856695 | 15:74,593,253 | A/G | upstream gene variant | — |
| rs2930291 | 15:74,604,834 | G/C | — | — |
| rs56372559 | 15:74,606,238 | G/A | intron variant | — |
| rs2959011 | 15:74,611,781 | A/C | — | — |
| rs733434 | 15:74,614,271 | A/G | intron variant | — |
| rs1564783 | 15:74,614,913 | G/A | — | — |
| rs2959008 | 15:74,616,577 | A/G | intron variant | — |
| rs756387713 | 15:74,622,545 | C/T | — | uncertain significance |
| rs780371126 | 15:74,622,546 | G/A | — | uncertain significance |
| rs749495036 | 15:74,622,548 | C/T | — | uncertain significance |
| rs748705543 | 15:74,622,565 | G/A | — | uncertain significance |
| rs758922892 | 15:74,622,581 | T/C | — | uncertain significance |
| rs2060401038 | 15:74,622,596 | G/A | — | likely benign |
| rs755196411 | 15:74,622,627 | T/C | — | uncertain significance |
| rs201777513 | 15:74,622,693 | C/T | — | likely benign |
| rs751880673 | 15:74,623,009 | A/C | — | uncertain significance |
| rs1245753508 | 15:74,623,074 | G/T | — | uncertain significance |
| rs766863738 | 15:74,623,332 | G/A | — | uncertain significance |
| rs368022401 | 15:74,623,361 | G/T | — | uncertain significance |
| rs368665468 | 15:74,623,439 | C/T | — | uncertain significance |
| rs539124387 | 15:74,623,550 | G/A | — | uncertain significance |
| rs199573669 | 15:74,623,556 | A/G | — | uncertain significance |
| rs945225317 | 15:74,623,580 | C/G | — | uncertain significance |
| rs754809994 | 15:74,623,635 | C/T | — | likely benign |
| rs146131430 | 15:74,625,025 | C/T | — | uncertain significance |
| rs77396610 | 15:74,625,077 | C/T | — | likely benign |
| rs567165147 | 15:74,625,109 | A/C | — | uncertain significance |
| rs900538519 | 15:74,625,113 | C/T | — | uncertain significance |
| rs184774328 | 15:74,625,121 | C/T | — | uncertain significance |
| rs201882376 | 15:74,625,125 | C/T | — | uncertain significance |
| rs745334657 | 15:74,625,142 | C/T | — | uncertain significance |
| rs746751133 | 15:74,626,255 | C/T | — | uncertain significance |
| rs2548319447 | 15:74,626,256 | T/A | — | uncertain significance |
| rs768822161 | 15:74,626,285 | C/T | — | uncertain significance |
| rs200097810 | 15:74,627,368 | G/A | — | uncertain significance |
| rs755898743 | 15:74,627,388 | G/T | — | uncertain significance |
| rs777898212 | 15:74,627,404 | C/T | — | uncertain significance |
| rs1360070501 | 15:74,628,300 | C/T | — | uncertain significance |
| rs2959003 | 15:74,628,891 | A/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.