WDR76
WD repeat domain 76
Summary
Enables enzyme binding activity. Involved in DNA damage response. Located in heterochromatin; nucleus; and site of DNA damage. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs185884229 | 15:44,119,666 | C/T | upstream gene variant | — |
| rs751456124 | 15:44,120,214 | G/T | — | uncertain significance |
| rs200562387 | 15:44,120,256 | G/T | — | uncertain significance |
| rs766284931 | 15:44,120,363 | G/T | — | uncertain significance |
| rs751542493 | 15:44,120,454 | A/G | — | uncertain significance |
| rs2508040432 | 15:44,127,305 | T/C | — | uncertain significance |
| rs377752604 | 15:44,128,374 | C/T | — | uncertain significance |
| rs970854697 | 15:44,131,846 | A/G | — | uncertain significance |
| rs1282788555 | 15:44,131,879 | T/A | — | uncertain significance |
| rs146758589 | 15:44,131,911 | A/T | — | uncertain significance |
| rs201894093 | 15:44,134,668 | A/G | — | likely benign |
| rs2087737024 | 15:44,134,680 | A/G | — | uncertain significance |
| rs2508064446 | 15:44,134,682 | G/C | — | uncertain significance |
| rs771930301 | 15:44,136,166 | A/G | — | likely benign |
| rs758766580 | 15:44,136,215 | T/C | — | likely benign |
| rs549630577 | 15:44,143,295 | C/A | — | uncertain significance |
| rs2087854718 | 15:44,143,367 | A/G | — | uncertain significance |
| rs28413704 | 15:44,148,427 | A/G | intron variant | — |
| rs748958193 | 15:44,149,144 | G/A | — | uncertain significance |
| rs779575395 | 15:44,149,283 | C/A | — | uncertain significance |
| rs770124440 | 15:44,149,300 | A/G | — | uncertain significance |
| rs1486136713 | 15:44,149,323 | C/G | — | uncertain significance |
| rs373881361 | 15:44,153,544 | A/G | — | uncertain significance |
| rs143768542 | 15:44,153,568 | C/T | — | uncertain significance |
| rs150494621 | 15:44,153,571 | C/T | missense variant | — |
| rs139843108 | 15:44,158,346 | G/A | — | uncertain significance |
| rs146664124 | 15:44,158,394 | G/C | — | uncertain significance |
| rs763434356 | 15:44,158,427 | G/A | — | uncertain significance |
| rs766811074 | 15:44,158,442 | A/G | — | uncertain significance |
| rs755745847 | 15:44,158,445 | A/C | — | uncertain significance |
| rs745752918 | 15:44,158,483 | C/T | — | uncertain significance |
| rs777400816 | 15:44,158,492 | G/C | — | uncertain significance |
| rs753472459 | 15:44,158,522 | C/T | — | uncertain significance |
| rs769298819 | 15:44,158,529 | T/G | — | uncertain significance |
| rs2508149976 | 15:44,158,544 | A/C | — | uncertain significance |
| rs759938560 | 15:44,158,572 | G/T | — | uncertain significance |
| rs767669645 | 15:44,158,577 | A/G | — | uncertain significance |
| rs541871 | 15:44,160,854 | G/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.