WDR93
WD repeat domain 93
Summary
Predicted to be involved in electron transport chain. Predicted to be part of respiratory chain complex I. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2505621233 | 15:90,244,996 | A/T | — | uncertain significance |
| rs2505621471 | 15:90,245,021 | C/T | — | uncertain significance |
| rs373758152 | 15:90,245,024 | T/C | — | uncertain significance |
| rs779370026 | 15:90,245,167 | G/C | — | uncertain significance |
| rs730882204 | 15:90,245,257 | T/C | missense variant | pathogenic |
| rs758900957 | 15:90,245,263 | C/G | — | uncertain significance |
| rs200060975 | 15:90,248,844 | G/A | — | uncertain significance |
| rs750414405 | 15:90,255,294 | A/G | — | uncertain significance |
| rs376704792 | 15:90,258,216 | G/A | — | uncertain significance |
| rs1451462203 | 15:90,258,231 | G/C | — | uncertain significance |
| rs1227288745 | 15:90,258,264 | A/G | — | uncertain significance |
| rs2505676846 | 15:90,258,286 | T/C | — | uncertain significance |
| rs201947112 | 15:90,258,306 | A/G | — | uncertain significance |
| rs369766149 | 15:90,258,319 | C/T | — | likely benign |
| rs201614814 | 15:90,258,324 | C/A | — | uncertain significance |
| rs139621549 | 15:90,262,689 | T/C | intron variant | — |
| rs760170946 | 15:90,265,324 | T/C | — | uncertain significance |
| rs1966551870 | 15:90,265,352 | C/G | — | uncertain significance |
| rs142701744 | 15:90,269,916 | A/T | intron variant | — |
| rs544888295 | 15:90,270,175 | G/A | — | — |
| rs560024697 | 15:90,270,404 | C/T | — | likely benign |
| rs1966773107 | 15:90,270,451 | C/A | — | uncertain significance |
| rs769426748 | 15:90,270,510 | G/A | — | uncertain significance |
| rs568009086 | 15:90,270,562 | G/A | — | likely benign |
| rs779540687 | 15:90,272,271 | T/G | — | uncertain significance |
| rs776824082 | 15:90,272,304 | C/T | — | uncertain significance |
| rs2505734721 | 15:90,272,968 | A/G | — | uncertain significance |
| rs756462572 | 15:90,273,862 | C/T | — | — |
| rs1388682181 | 15:90,274,767 | T/G | — | uncertain significance |
| rs2505749034 | 15:90,276,350 | A/G | — | uncertain significance |
| rs573471914 | 15:90,276,386 | G/A | — | uncertain significance |
| rs2505749534 | 15:90,276,441 | T/C | — | uncertain significance |
| rs753524261 | 15:90,280,900 | G/A | — | uncertain significance |
| rs371255543 | 15:90,281,275 | A/G | — | uncertain significance |
| rs180930292 | 15:90,281,352 | C/T | — | uncertain significance |
| rs373980931 | 15:90,281,353 | C/T | — | uncertain significance |
| rs144543841 | 15:90,281,422 | A/C | — | uncertain significance |
| rs143711734 | 15:90,286,525 | A/C | — | uncertain significance |
| rs147211563 | 15:90,286,528 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.