DRC3
dynein regulatory complex subunit 3
Summary
Located in axoneme. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs367593570 | 17:17,880,933 | G/T | — | likely benign |
| rs267604763 | 17:17,880,955 | G/A | — | uncertain significance |
| rs746958523 | 17:17,880,976 | G/A | — | uncertain significance |
| rs187632732 | 17:17,887,142 | A/G | — | uncertain significance |
| rs1439176060 | 17:17,887,144 | A/G | — | uncertain significance |
| rs193222617 | 17:17,887,186 | A/G | — | likely benign |
| rs201063688 | 17:17,887,226 | G/T | — | uncertain significance |
| rs751283013 | 17:17,887,249 | G/C | — | uncertain significance |
| rs184914676 | 17:17,889,473 | G/A | upstream gene variant | — |
| rs1234676613 | 17:17,891,272 | A/G | — | uncertain significance |
| rs536193055 | 17:17,891,327 | G/A | — | uncertain significance |
| rs202136595 | 17:17,891,359 | G/A | — | uncertain significance |
| rs781422305 | 17:17,891,384 | G/A | — | uncertain significance |
| rs568705588 | 17:17,892,227 | C/T | — | — |
| rs554588749 | 17:17,896,208 | C/T | — | uncertain significance |
| rs185967799 | 17:17,896,209 | G/A | — | uncertain significance |
| rs761307066 | 17:17,897,673 | C/G | — | uncertain significance |
| rs1181998889 | 17:17,897,682 | G/A | — | uncertain significance |
| rs747487490 | 17:17,897,693 | G/C | — | uncertain significance |
| rs1342146355 | 17:17,897,704 | C/T | — | uncertain significance |
| rs750680393 | 17:17,897,709 | C/T | — | uncertain significance |
| rs547331351 | 17:17,898,341 | C/T | — | uncertain significance |
| rs181839904 | 17:17,900,856 | G/A | — | uncertain significance |
| rs199972472 | 17:17,900,878 | G/A | — | likely benign |
| rs62072049 | 17:17,906,520 | T/A | — | — |
| rs1179243512 | 17:17,907,774 | T/A | — | uncertain significance |
| rs375064299 | 17:17,909,512 | T/C | — | uncertain significance |
| rs200313075 | 17:17,909,524 | A/G | — | uncertain significance |
| rs772644849 | 17:17,909,555 | A/C | — | uncertain significance |
| rs1272872199 | 17:17,910,352 | G/A | — | uncertain significance |
| rs201906441 | 17:17,910,447 | A/G | — | likely benign |
| rs200124645 | 17:17,910,448 | A/G | — | uncertain significance |
| rs200381151 | 17:17,919,414 | G/A | — | likely benign |
| rs748163277 | 17:17,919,438 | C/G | — | uncertain significance |
| rs759026512 | 17:17,919,475 | G/T | — | uncertain significance |
| rs1207384684 | 17:17,919,880 | G/C | — | uncertain significance |
| rs368791219 | 17:17,919,900 | G/A | — | uncertain significance |
| rs375162242 | 17:17,919,905 | C/T | — | uncertain significance |
| rs766718133 | 17:17,919,932 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.