CCDC17
coiled-coil domain containing 17
Summary
Implicated in colorectal adenocarcinoma. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs61789988 | 1:46,085,242 | G/C | — | — |
| rs558957246 | 1:46,086,006 | C/G | — | uncertain significance |
| rs142888180 | 1:46,086,042 | G/A | — | uncertain significance |
| rs3014246 | 1:46,086,077 | C/T | missense variant | — |
| rs779809298 | 1:46,086,096 | T/A | — | likely benign |
| rs2148385206 | 1:46,086,105 | C/T | — | uncertain significance |
| rs764795876 | 1:46,086,481 | G/A | — | uncertain significance |
| rs1021784302 | 1:46,086,604 | T/C | — | uncertain significance |
| rs749615206 | 1:46,086,643 | G/A | — | uncertain significance |
| rs201008298 | 1:46,086,649 | G/A | — | uncertain significance |
| rs377018471 | 1:46,086,654 | C/G | — | uncertain significance |
| rs2297655 | 1:46,086,663 | C/T | — | uncertain significance |
| rs374329461 | 1:46,086,664 | G/A | — | uncertain significance |
| rs17410855 | 1:46,086,766 | T/C | — | benign |
| rs139210753 | 1:46,086,987 | A/C | — | uncertain significance |
| rs1444929495 | 1:46,087,022 | A/C | — | uncertain significance |
| rs2522157636 | 1:46,087,039 | C/A | — | uncertain significance |
| rs781307741 | 1:46,087,043 | G/A | — | uncertain significance |
| rs369609741 | 1:46,087,065 | G/A | — | uncertain significance |
| rs1644250443 | 1:46,087,067 | C/T | — | uncertain significance |
| rs770745084 | 1:46,087,071 | C/A | — | uncertain significance |
| rs200507548 | 1:46,087,073 | C/A | — | uncertain significance |
| rs201021595 | 1:46,087,313 | G/C | — | uncertain significance |
| rs780733912 | 1:46,087,331 | C/A | — | uncertain significance |
| rs1454289997 | 1:46,087,337 | A/G | — | uncertain significance |
| rs765234623 | 1:46,087,370 | A/G | — | uncertain significance |
| rs745748431 | 1:46,087,605 | G/A | — | uncertain significance |
| rs374103555 | 1:46,087,609 | A/T | — | uncertain significance |
| rs771125808 | 1:46,087,639 | A/C | — | uncertain significance |
| rs893571511 | 1:46,087,644 | C/T | — | uncertain significance |
| rs1157119790 | 1:46,087,652 | C/T | — | uncertain significance |
| rs762460789 | 1:46,087,925 | G/A | — | uncertain significance |
| rs764528145 | 1:46,087,936 | A/T | — | uncertain significance |
| rs746935513 | 1:46,087,969 | C/T | — | likely benign |
| rs1414580168 | 1:46,088,014 | G/C | — | uncertain significance |
| rs375560678 | 1:46,088,441 | G/A | — | uncertain significance |
| rs770151819 | 1:46,088,447 | G/A | — | uncertain significance |
| rs1312730144 | 1:46,088,462 | A/T | — | uncertain significance |
| rs763870322 | 1:46,088,499 | G/T | — | uncertain significance |
| rs774726919 | 1:46,088,691 | C/T | — | uncertain significance |
| rs1557680538 | 1:46,088,693 | G/A | — | uncertain significance |
| rs754560155 | 1:46,088,756 | G/T | — | uncertain significance |
| rs1217644933 | 1:46,088,945 | G/A | — | uncertain significance |
| rs747359235 | 1:46,088,946 | C/T | — | uncertain significance |
| rs1211646992 | 1:46,089,011 | T/C | — | uncertain significance |
| rs559955057 | 1:46,089,026 | G/C | — | uncertain significance |
| rs534181097 | 1:46,089,095 | A/G | — | uncertain significance |
| rs973833846 | 1:46,089,244 | C/G | — | uncertain significance |
| rs2522233473 | 1:46,089,276 | G/C | — | uncertain significance |
| rs755360041 | 1:46,089,287 | G/T | — | uncertain significance |
| rs1644361153 | 1:46,089,321 | C/T | — | uncertain significance |
| rs2522238127 | 1:46,089,431 | C/A | — | uncertain significance |
| rs908069181 | 1:46,089,520 | C/T | — | uncertain significance |
| rs77131772 | 1:46,090,719 | T/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.