CCDC18
coiled-coil domain containing 18
Summary
Located in centriolar satellite. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants91 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs202201009 | 1:93,649,035 | A/G | — | likely benign |
| rs2524313148 | 1:93,649,535 | T/A | — | uncertain significance |
| rs537114111 | 1:93,649,545 | A/C | — | uncertain significance |
| rs2524313602 | 1:93,649,546 | G/A | — | uncertain significance |
| rs1238436494 | 1:93,649,569 | A/G | — | uncertain significance |
| rs2524322263 | 1:93,649,686 | A/G | — | uncertain significance |
| rs74596359 | 1:93,651,922 | T/C | — | benign |
| rs777431171 | 1:93,652,007 | T/A | — | uncertain significance |
| rs199719529 | 1:93,652,057 | A/G | — | likely benign |
| rs201703475 | 1:93,657,581 | C/G | — | uncertain significance |
| rs775269081 | 1:93,657,614 | C/A | — | uncertain significance |
| rs115246469 | 1:93,657,672 | A/G | — | benign |
| rs11164880 | 1:93,658,096 | A/C | upstream gene variant | — |
| rs2524586296 | 1:93,659,273 | T/G | — | uncertain significance |
| rs2524782085 | 1:93,667,493 | T/C | — | uncertain significance |
| rs2783499 | 1:93,672,688 | C/T | — | benign |
| rs2815413 | 1:93,672,723 | A/C | — | benign |
| rs1464927711 | 1:93,672,814 | C/A | — | likely benign |
| rs199887942 | 1:93,672,827 | A/G | — | uncertain significance |
| rs201200084 | 1:93,672,840 | G/A | — | uncertain significance |
| rs185365289 | 1:93,672,855 | G/A | — | uncertain significance |
| rs958260544 | 1:93,672,870 | A/G | — | uncertain significance |
| rs780524469 | 1:93,672,908 | T/A | — | uncertain significance |
| rs1217419068 | 1:93,676,402 | A/G | — | uncertain significance |
| rs185127229 | 1:93,676,434 | C/T | — | benign |
| rs189830464 | 1:93,676,439 | C/T | — | benign |
| rs2525053793 | 1:93,676,440 | A/G | — | uncertain significance |
| rs745699922 | 1:93,676,455 | G/A | — | uncertain significance |
| rs750546126 | 1:93,676,467 | G/A | — | likely benign |
| rs76148185 | 1:93,676,478 | A/C | — | benign |
| rs1451646714 | 1:93,677,665 | C/T | — | uncertain significance |
| rs200393545 | 1:93,677,666 | T/C | — | likely benign |
| rs1360879955 | 1:93,677,714 | C/G | — | uncertain significance |
| rs183557342 | 1:93,677,754 | C/A | — | uncertain significance |
| rs188439846 | 1:93,677,761 | A/G | — | likely benign |
| rs200273930 | 1:93,677,792 | C/A | — | likely benign |
| rs2525180854 | 1:93,680,327 | A/G | — | uncertain significance |
| rs376962690 | 1:93,680,371 | A/C | — | uncertain significance |
| rs1235508870 | 1:93,680,372 | C/T | — | uncertain significance |
| rs1656231788 | 1:93,680,430 | G/T | — | uncertain significance |
| rs1278113782 | 1:93,680,441 | T/C | — | uncertain significance |
| rs761037021 | 1:93,680,473 | C/G | — | uncertain significance |
| rs112836442 | 1:93,680,515 | G/A | — | likely benign |
| rs373731787 | 1:93,682,224 | T/C | — | uncertain significance |
| rs1656749253 | 1:93,683,325 | A/G | — | uncertain significance |
| rs757597480 | 1:93,683,368 | A/T | — | uncertain significance |
| rs768472646 | 1:93,683,407 | T/C | — | uncertain significance |
| rs201591350 | 1:93,687,213 | A/G | — | likely benign |
| rs766811138 | 1:93,687,287 | C/A | — | uncertain significance |
| rs138388409 | 1:93,687,288 | G/A | — | likely benign |
| rs200891592 | 1:93,687,292 | A/G | — | uncertain significance |
| rs752186690 | 1:93,687,439 | G/C | — | uncertain significance |
| rs778057310 | 1:93,691,881 | C/T | — | likely benign |
| rs775654467 | 1:93,691,905 | T/G | — | uncertain significance |
| rs766262826 | 1:93,691,947 | A/C | — | uncertain significance |
| rs755358660 | 1:93,698,019 | C/G | — | uncertain significance |
| rs763008846 | 1:93,698,071 | A/C | — | uncertain significance |
| rs77458693 | 1:93,698,072 | G/A | — | benign |
| rs373322065 | 1:93,698,088 | T/G | — | uncertain significance |
| rs78187035 | 1:93,698,141 | T/G | — | benign |
| rs761725681 | 1:93,701,866 | A/G | — | uncertain significance |
| rs1172354895 | 1:93,701,926 | T/C | — | uncertain significance |
| rs373433241 | 1:93,701,940 | A/G | — | uncertain significance |
| rs778632935 | 1:93,704,895 | A/G | — | uncertain significance |
| rs199941655 | 1:93,704,941 | G/A | — | uncertain significance |
| rs41292127 | 1:93,704,952 | A/G | — | benign |
| rs2525994772 | 1:93,704,970 | T/C | — | uncertain significance |
| rs190190295 | 1:93,705,291 | C/T | — | uncertain significance |
| rs565919 | 1:93,706,713 | C/A | — | — |
| rs754773122 | 1:93,711,656 | T/C | — | likely benign |
| rs996388310 | 1:93,711,679 | T/C | — | uncertain significance |
| rs201175141 | 1:93,712,465 | G/C | — | uncertain significance |
| rs797680 | 1:93,716,974 | G/T | intron variant | — |
| rs12030843 | 1:93,720,070 | C/G | — | benign |
| rs61729705 | 1:93,720,153 | G/A | — | benign |
| rs779762735 | 1:93,721,991 | C/A | — | uncertain significance |
| rs771005543 | 1:93,722,013 | G/A | — | uncertain significance |
| rs112487174 | 1:93,722,055 | C/T | — | uncertain significance |
| rs183806092 | 1:93,724,353 | C/A | — | uncertain significance |
| rs367601314 | 1:93,730,259 | T/C | — | uncertain significance |
| rs2526803689 | 1:93,730,298 | C/T | — | uncertain significance |
| rs754019429 | 1:93,730,370 | A/C | — | uncertain significance |
| rs139422966 | 1:93,730,380 | T/A | — | benign |
| rs752805708 | 1:93,730,381 | A/G | — | uncertain significance |
| rs747191589 | 1:93,730,413 | T/C | — | likely benign |
| rs150053356 | 1:93,730,416 | G/A | — | benign |
| rs2526809445 | 1:93,730,424 | T/C | — | uncertain significance |
| rs2526810876 | 1:93,730,456 | A/G | — | uncertain significance |
| rs41292129 | 1:93,735,934 | A/T | — | benign |
| rs375334492 | 1:93,736,290 | T/C | — | likely benign |
| rs2296558 | 1:93,736,555 | C/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.