CCDC3
coiled-coil domain containing 3
Summary
Involved in negative regulation of lipid metabolic process; negative regulation of tumor necrosis factor-mediated signaling pathway; and signal transduction. Located in endoplasmic reticulum and extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs374419795 | 10:12,940,429 | T/G | — | uncertain significance |
| rs116856516 | 10:12,940,432 | T/G | — | uncertain significance |
| rs1834040930 | 10:12,940,457 | T/G | — | uncertain significance |
| rs758296205 | 10:12,940,458 | G/C | — | uncertain significance |
| rs371834557 | 10:12,940,480 | G/A | — | uncertain significance |
| rs201286626 | 10:12,940,522 | C/A | — | uncertain significance |
| rs749951291 | 10:12,940,544 | G/A | — | uncertain significance |
| rs779643128 | 10:12,940,561 | T/A | — | uncertain significance |
| rs748960897 | 10:12,940,562 | T/C | — | uncertain significance |
| rs767395696 | 10:12,940,592 | G/A | — | uncertain significance |
| rs4748011 | 10:12,941,157 | T/C | intron variant | association |
| rs35859988 | 10:12,944,646 | C/T | regulatory region variant | — |
| rs34321514 | 10:12,949,653 | G/T | — | — |
| rs1659850 | 10:12,982,925 | G/T | intron variant | — |
| rs563209158 | 10:13,019,800 | T/C | — | — |
| rs150962471 | 10:13,025,734 | G/A | regulatory region variant | — |
| rs754383912 | 10:13,040,371 | G/T | — | uncertain significance |
| rs144679549 | 10:13,040,378 | G/A | — | likely benign |
| rs760041673 | 10:13,043,222 | C/T | — | uncertain significance |
| rs775862668 | 10:13,043,230 | A/C | — | uncertain significance |
| rs1407582274 | 10:13,043,264 | C/A | — | uncertain significance |
| rs1365420712 | 10:13,043,405 | G/A | — | uncertain significance |
| rs1835852132 | 10:13,043,413 | G/A | — | uncertain significance |
| rs1169425720 | 10:13,043,473 | T/G | — | uncertain significance |
| rs1041812863 | 10:13,043,485 | C/T | — | uncertain significance |
| rs891270190 | 10:13,043,515 | G/A | — | uncertain significance |
| rs974083043 | 10:13,043,528 | G/T | — | uncertain significance |
| rs564190838 | 10:13,043,530 | C/T | — | uncertain significance |
| rs525455 | 10:13,103,285 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.