CCDC158
coiled-coil domain containing 158
Known Variants78 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200464150 | 4:77,234,376 | G/T | — | uncertain significance |
| rs202034960 | 4:77,234,394 | A/G | — | uncertain significance |
| rs2476577021 | 4:77,244,461 | T/C | — | uncertain significance |
| rs771256504 | 4:77,244,463 | T/C | — | uncertain significance |
| rs1350467718 | 4:77,244,523 | C/A | — | uncertain significance |
| rs767872164 | 4:77,247,045 | G/A | — | uncertain significance |
| rs576903605 | 4:77,247,090 | G/A | — | uncertain significance |
| rs1720489882 | 4:77,247,102 | T/G | — | uncertain significance |
| rs201687534 | 4:77,247,129 | T/C | — | uncertain significance |
| rs375412402 | 4:77,247,138 | C/T | — | uncertain significance |
| rs558880123 | 4:77,250,109 | G/C | — | uncertain significance |
| rs780320632 | 4:77,252,509 | T/G | — | uncertain significance |
| rs778561830 | 4:77,252,536 | T/C | — | uncertain significance |
| rs765722805 | 4:77,255,206 | C/T | — | uncertain significance |
| rs751171490 | 4:77,255,220 | G/A | — | uncertain significance |
| rs1722989553 | 4:77,272,183 | G/A | — | uncertain significance |
| rs2476942388 | 4:77,272,208 | C/T | — | uncertain significance |
| rs759046733 | 4:77,272,228 | C/T | — | uncertain significance |
| rs377167162 | 4:77,272,259 | C/T | — | uncertain significance |
| rs375808480 | 4:77,272,904 | C/T | — | uncertain significance |
| rs909965143 | 4:77,272,943 | C/T | — | uncertain significance |
| rs200019740 | 4:77,274,319 | C/T | — | uncertain significance |
| rs781102118 | 4:77,274,382 | G/C | — | uncertain significance |
| rs369022560 | 4:77,276,502 | T/C | — | uncertain significance |
| rs750348114 | 4:77,276,578 | C/G | — | uncertain significance |
| rs1723681643 | 4:77,278,581 | C/G | — | uncertain significance |
| rs1379412385 | 4:77,278,589 | G/A | — | uncertain significance |
| rs200928353 | 4:77,278,649 | C/T | — | uncertain significance |
| rs749803167 | 4:77,278,668 | C/T | — | uncertain significance |
| rs368420803 | 4:77,283,402 | C/T | — | uncertain significance |
| rs758950777 | 4:77,283,437 | C/T | — | uncertain significance |
| rs371552188 | 4:77,283,438 | G/A | — | uncertain significance |
| rs756860152 | 4:77,283,442 | C/A | — | uncertain significance |
| rs138981058 | 4:77,284,527 | C/T | intron variant | — |
| rs908317338 | 4:77,288,474 | A/C | — | uncertain significance |
| rs149717358 | 4:77,288,502 | T/A | — | uncertain significance |
| rs2477256456 | 4:77,288,641 | C/A | — | uncertain significance |
| rs201262548 | 4:77,288,683 | C/T | — | uncertain significance |
| rs200881803 | 4:77,288,725 | C/G | — | uncertain significance |
| rs1332508123 | 4:77,288,787 | G/A | — | uncertain significance |
| rs561723655 | 4:77,288,844 | C/T | — | uncertain significance |
| rs181312230 | 4:77,288,866 | C/G | — | uncertain significance |
| rs758631188 | 4:77,288,926 | C/T | — | uncertain significance |
| rs374158846 | 4:77,290,583 | C/T | — | uncertain significance |
| rs376921286 | 4:77,290,637 | C/T | — | uncertain significance |
| rs1329795418 | 4:77,290,655 | C/T | — | uncertain significance |
| rs775250551 | 4:77,290,709 | C/T | — | uncertain significance |
| rs374047426 | 4:77,292,581 | G/C | — | uncertain significance |
| rs371689241 | 4:77,292,608 | C/T | — | uncertain significance |
| rs759340288 | 4:77,292,625 | C/T | — | uncertain significance |
| rs2477339910 | 4:77,292,688 | G/A | — | likely benign |
| rs368826843 | 4:77,300,466 | C/A | — | uncertain significance |
| rs375811573 | 4:77,300,484 | G/A | — | uncertain significance |
| rs746185302 | 4:77,303,835 | G/A | — | uncertain significance |
| rs774435291 | 4:77,304,845 | A/G | — | uncertain significance |
| rs757207797 | 4:77,305,321 | G/A | — | uncertain significance |
| rs781065656 | 4:77,305,327 | G/A | — | uncertain significance |
| rs2477544807 | 4:77,305,351 | C/G | — | uncertain significance |
| rs751110311 | 4:77,305,398 | C/T | — | uncertain significance |
| rs369057239 | 4:77,305,399 | G/A | — | uncertain significance |
| rs1560456369 | 4:77,305,413 | A/T | — | uncertain significance |
| rs200015744 | 4:77,305,440 | C/T | — | uncertain significance |
| rs371546006 | 4:77,305,458 | G/A | — | uncertain significance |
| rs775899999 | 4:77,305,549 | G/T | — | uncertain significance |
| rs1356587071 | 4:77,305,713 | T/C | — | uncertain significance |
| rs1013402669 | 4:77,305,749 | G/C | — | uncertain significance |
| rs770409315 | 4:77,305,769 | A/G | — | uncertain significance |
| rs55948430 | 4:77,308,705 | C/T | intron variant | — |
| rs749241147 | 4:77,317,505 | G/T | — | uncertain significance |
| rs761629412 | 4:77,317,522 | G/A | — | uncertain significance |
| rs943243229 | 4:77,317,525 | T/C | — | uncertain significance |
| rs745598725 | 4:77,317,564 | G/A | — | uncertain significance |
| rs2477733956 | 4:77,317,585 | G/A | — | uncertain significance |
| rs368025660 | 4:77,317,606 | C/T | — | uncertain significance |
| rs201063324 | 4:77,317,607 | G/A | — | uncertain significance |
| rs374895901 | 4:77,317,610 | T/C | — | uncertain significance |
| rs762442108 | 4:77,324,326 | T/A | — | uncertain significance |
| rs140797179 | 4:77,324,978 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.