CCDC157
coiled-coil domain containing 157
Known Variants59 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs5753093 | 22:30,755,172 | A/C | upstream gene variant | — |
| rs557415482 | 22:30,762,015 | C/G | — | uncertain significance |
| rs773932430 | 22:30,762,032 | C/T | — | uncertain significance |
| rs374803463 | 22:30,762,086 | G/A | — | uncertain significance |
| rs200955387 | 22:30,762,095 | C/T | — | uncertain significance |
| rs201763455 | 22:30,762,123 | G/A | — | uncertain significance |
| rs778897051 | 22:30,762,134 | G/A | — | uncertain significance |
| rs529483498 | 22:30,762,177 | C/T | — | uncertain significance |
| rs151177194 | 22:30,762,180 | G/A | — | uncertain significance |
| rs766620698 | 22:30,762,188 | G/A | — | uncertain significance |
| rs147104395 | 22:30,762,234 | A/G | — | uncertain significance |
| rs770842176 | 22:30,765,533 | C/T | — | uncertain significance |
| rs753449486 | 22:30,765,537 | G/A | — | uncertain significance |
| rs780299712 | 22:30,765,559 | G/C | — | uncertain significance |
| rs760637343 | 22:30,765,582 | C/T | — | uncertain significance |
| rs767712736 | 22:30,766,346 | C/A | — | uncertain significance |
| rs143249037 | 22:30,766,366 | G/A | — | uncertain significance |
| rs150581663 | 22:30,766,444 | T/C | — | uncertain significance |
| rs139609945 | 22:30,766,496 | C/T | — | uncertain significance |
| rs141091935 | 22:30,766,698 | G/A | — | likely benign |
| rs749724460 | 22:30,766,726 | G/A | — | uncertain significance |
| rs145673028 | 22:30,766,747 | C/T | — | uncertain significance |
| rs547209278 | 22:30,766,792 | G/A | — | uncertain significance |
| rs1569189218 | 22:30,766,843 | G/A | — | uncertain significance |
| rs770367866 | 22:30,768,094 | G/C | — | likely benign |
| rs745435347 | 22:30,768,100 | G/A | — | uncertain significance |
| rs2518306826 | 22:30,768,169 | A/C | — | uncertain significance |
| rs777556030 | 22:30,768,193 | G/C | — | uncertain significance |
| rs142435200 | 22:30,768,223 | C/T | — | uncertain significance |
| rs1033062204 | 22:30,769,593 | A/G | — | uncertain significance |
| rs2518320741 | 22:30,769,623 | T/G | — | uncertain significance |
| rs569921570 | 22:30,769,644 | G/A | — | uncertain significance |
| rs201264202 | 22:30,769,670 | G/A | — | uncertain significance |
| rs766248109 | 22:30,769,686 | G/A | — | uncertain significance |
| rs753736532 | 22:30,769,699 | G/C | — | uncertain significance |
| rs746192462 | 22:30,769,719 | G/A | — | uncertain significance |
| rs376030866 | 22:30,769,743 | G/C | — | uncertain significance |
| rs747260037 | 22:30,769,958 | C/T | — | likely benign |
| rs150205621 | 22:30,769,964 | C/T | — | uncertain significance |
| rs775533622 | 22:30,769,972 | C/T | — | uncertain significance |
| rs143181893 | 22:30,769,996 | C/T | — | uncertain significance |
| rs749261960 | 22:30,770,029 | C/A | — | uncertain significance |
| rs1933159000 | 22:30,770,062 | A/G | — | uncertain significance |
| rs545605224 | 22:30,770,078 | A/G | — | uncertain significance |
| rs368250287 | 22:30,771,567 | G/A | — | uncertain significance |
| rs758242089 | 22:30,771,572 | C/T | — | uncertain significance |
| rs2518342634 | 22:30,771,579 | T/C | — | uncertain significance |
| rs111283506 | 22:30,771,596 | C/T | — | uncertain significance |
| rs1367145156 | 22:30,771,644 | G/A | — | uncertain significance |
| rs753475863 | 22:30,772,255 | C/T | — | uncertain significance |
| rs1012644209 | 22:30,772,263 | C/T | — | uncertain significance |
| rs139750381 | 22:30,772,457 | C/T | — | uncertain significance |
| rs754954495 | 22:30,772,475 | G/C | — | uncertain significance |
| rs185099385 | 22:30,772,570 | C/T | — | uncertain significance |
| rs2518356131 | 22:30,772,670 | A/G | — | likely benign |
| rs150705487 | 22:30,772,687 | C/G | — | uncertain significance |
| rs1316315321 | 22:30,772,715 | C/A | — | uncertain significance |
| rs1275308129 | 22:30,772,723 | C/T | — | uncertain significance |
| rs761836101 | 22:30,772,724 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.