CCDC60
coiled-coil domain containing 60
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11064768 | 12:119,818,509 | A/G | intron variant | — |
| rs541650762 | 12:119,818,690 | G/C | — | — |
| rs2500179804 | 12:119,866,526 | C/G | — | uncertain significance |
| rs576781017 | 12:119,866,530 | G/C | — | uncertain significance |
| rs200214070 | 12:119,866,545 | A/G | — | uncertain significance |
| rs761390907 | 12:119,866,567 | G/A | — | uncertain significance |
| rs1520758 | 12:119,891,617 | C/G | — | — |
| rs755757512 | 12:119,909,806 | A/G | — | uncertain significance |
| rs755919639 | 12:119,909,915 | A/C | — | uncertain significance |
| rs377075044 | 12:119,916,954 | T/C | — | uncertain significance |
| rs762470910 | 12:119,916,965 | C/G | — | uncertain significance |
| rs144745942 | 12:119,926,565 | G/A | — | uncertain significance |
| rs147505092 | 12:119,926,577 | C/T | — | uncertain significance |
| rs1057223024 | 12:119,926,628 | A/G | — | uncertain significance |
| rs1232548802 | 12:119,926,633 | C/G | — | uncertain significance |
| rs1951813804 | 12:119,937,947 | T/G | — | uncertain significance |
| rs780719474 | 12:119,942,900 | G/A | — | uncertain significance |
| rs747656084 | 12:119,942,901 | C/G | — | uncertain significance |
| rs1352777904 | 12:119,942,932 | G/T | — | uncertain significance |
| rs758216401 | 12:119,942,959 | G/T | — | uncertain significance |
| rs760703876 | 12:119,942,961 | G/C | — | uncertain significance |
| rs200185960 | 12:119,954,455 | G/A | — | uncertain significance |
| rs148047293 | 12:119,954,466 | C/T | — | uncertain significance |
| rs778828974 | 12:119,957,943 | A/G | — | likely benign |
| rs139069574 | 12:119,960,772 | A/G | — | uncertain significance |
| rs201339940 | 12:119,961,502 | A/G | — | uncertain significance |
| rs529146936 | 12:119,961,551 | T/C | — | uncertain significance |
| rs770253612 | 12:119,961,608 | T/C | — | uncertain significance |
| rs199921208 | 12:119,966,452 | G/A | — | likely benign |
| rs573242338 | 12:119,966,532 | G/A | — | uncertain significance |
| rs766116584 | 12:119,968,696 | C/T | — | uncertain significance |
| rs759169633 | 12:119,968,710 | G/A | — | uncertain significance |
| rs148787992 | 12:119,968,713 | C/A | — | uncertain significance |
| rs146415894 | 12:119,968,726 | G/A | — | uncertain significance |
| rs201822827 | 12:119,968,866 | G/C | — | uncertain significance |
| rs766738432 | 12:119,978,420 | T/G | — | uncertain significance |
| rs888851373 | 12:119,978,461 | A/G | — | uncertain significance |
| rs145014443 | 12:119,978,480 | G/A | — | uncertain significance |
| rs745836865 | 12:119,978,495 | T/C | — | uncertain significance |
| rs149106624 | 12:119,978,507 | G/T | — | uncertain significance |
| rs201432672 | 12:119,978,509 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.