CCDC71
coiled-coil domain containing 71
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs774180246 | 3:49,200,279 | C/T | — | uncertain significance |
| rs201199266 | 3:49,200,297 | G/A | — | uncertain significance |
| rs770588176 | 3:49,200,362 | C/T | — | uncertain significance |
| rs369053039 | 3:49,200,426 | G/A | — | uncertain significance |
| rs746590972 | 3:49,200,455 | G/A | — | uncertain significance |
| rs370024275 | 3:49,200,473 | C/T | — | uncertain significance |
| rs774662712 | 3:49,200,482 | C/T | — | uncertain significance |
| rs148872443 | 3:49,200,497 | C/T | — | likely benign |
| rs757326482 | 3:49,200,509 | C/T | — | uncertain significance |
| rs1464526080 | 3:49,200,524 | C/T | — | uncertain significance |
| rs201052008 | 3:49,200,573 | G/A | — | uncertain significance |
| rs761047613 | 3:49,200,578 | A/G | — | uncertain significance |
| rs773425388 | 3:49,200,762 | G/A | — | likely benign |
| rs760435661 | 3:49,200,800 | G/C | — | uncertain significance |
| rs945805555 | 3:49,200,836 | C/T | — | likely benign |
| rs370573313 | 3:49,200,839 | C/T | — | likely benign |
| rs2472592751 | 3:49,200,858 | T/A | — | uncertain significance |
| rs145288601 | 3:49,200,893 | C/T | — | likely benign |
| rs1316060881 | 3:49,200,965 | T/C | — | uncertain significance |
| rs772931427 | 3:49,200,972 | G/A | — | uncertain significance |
| rs144680166 | 3:49,201,046 | T/C | — | uncertain significance |
| rs1276972987 | 3:49,201,164 | C/T | — | uncertain significance |
| rs1247918303 | 3:49,201,259 | G/A | — | uncertain significance |
| rs769100705 | 3:49,201,266 | C/T | — | uncertain significance |
| rs2472593420 | 3:49,201,322 | A/G | — | uncertain significance |
| rs904389494 | 3:49,201,328 | G/C | — | uncertain significance |
| rs2472593527 | 3:49,201,422 | T/C | — | uncertain significance |
| rs1230183688 | 3:49,201,445 | C/T | — | uncertain significance |
| rs980736676 | 3:49,201,529 | C/T | — | uncertain significance |
| rs4499638 | 3:49,202,782 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.