CCDC69
coiled-coil domain containing 69
Summary
Predicted to enable microtubule binding activity. Involved in spindle midzone assembly. Located in spindle midzone. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs374122246 | 5:150,563,007 | G/A | — | likely benign |
| rs2532292164 | 5:150,563,083 | A/G | — | uncertain significance |
| rs765359505 | 5:150,563,093 | C/T | — | uncertain significance |
| rs778517045 | 5:150,563,131 | T/C | — | uncertain significance |
| rs746337448 | 5:150,563,134 | T/G | — | uncertain significance |
| rs180701365 | 5:150,563,153 | G/C | — | uncertain significance |
| rs764012830 | 5:150,563,174 | G/T | — | uncertain significance |
| rs376794089 | 5:150,563,965 | G/T | — | uncertain significance |
| rs748092478 | 5:150,565,027 | G/A | — | uncertain significance |
| rs761241013 | 5:150,565,082 | C/G | — | uncertain significance |
| rs367632765 | 5:150,565,601 | A/C | — | uncertain significance |
| rs1469649639 | 5:150,565,608 | G/T | — | uncertain significance |
| rs2532296965 | 5:150,566,955 | T/C | — | likely benign |
| rs751437294 | 5:150,566,988 | C/T | — | uncertain significance |
| rs746175735 | 5:150,567,014 | C/T | — | likely benign |
| rs114550607 | 5:150,572,362 | T/C | intron variant | — |
| rs191720914 | 5:150,572,474 | A/T | intron variant | — |
| rs562543205 | 5:150,572,640 | A/G | — | — |
| rs148835102 | 5:150,578,576 | T/A | — | uncertain significance |
| rs1752741754 | 5:150,578,581 | C/T | — | uncertain significance |
| rs200171089 | 5:150,581,147 | T/C | — | uncertain significance |
| rs768472982 | 5:150,581,150 | G/A | — | uncertain significance |
| rs1582045024 | 5:150,581,180 | T/C | — | uncertain significance |
| rs778077929 | 5:150,581,211 | G/A | — | uncertain significance |
| rs747546885 | 5:150,585,032 | C/T | — | likely benign |
| rs7724774 | 5:150,585,867 | G/A | intron variant | — |
| rs979455 | 5:150,594,802 | T/C | intron variant | — |
| rs761854152 | 5:150,603,496 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.