WDR3
WD repeat domain 3
Summary
This gene encodes a nuclear protein containing 10 WD repeats. WD repeats are approximately 30- to 40-amino acid domains containing several conserved residues, which usually include a trp-asp at the C-terminal end. Proteins belonging to the WD repeat family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. [provided by RefSeq, Jul 2008]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3754127 | 1:118,471,212 | C/T | upstream gene variant | — |
| rs376572237 | 1:118,475,967 | C/T | — | uncertain significance |
| rs1266269136 | 1:118,475,979 | A/T | — | uncertain significance |
| rs374993298 | 1:118,476,004 | G/C | — | uncertain significance |
| rs377392703 | 1:118,476,015 | A/G | — | uncertain significance |
| rs1308056118 | 1:118,476,037 | G/T | — | uncertain significance |
| rs371355148 | 1:118,476,042 | G/C | — | uncertain significance |
| rs200209712 | 1:118,476,052 | G/A | — | uncertain significance |
| rs904180684 | 1:118,476,070 | C/G | — | uncertain significance |
| rs1464165551 | 1:118,477,112 | G/T | — | uncertain significance |
| rs2525788210 | 1:118,477,237 | G/A | — | uncertain significance |
| rs767989957 | 1:118,477,280 | G/T | — | uncertain significance |
| rs772738618 | 1:118,479,441 | G/A | — | uncertain significance |
| rs751481934 | 1:118,479,491 | A/G | — | uncertain significance |
| rs3765501 | 1:118,479,749 | G/C | — | — |
| rs1182159402 | 1:118,481,146 | C/A | — | uncertain significance |
| rs537675666 | 1:118,483,496 | C/T | — | uncertain significance |
| rs200734934 | 1:118,483,748 | G/A | — | uncertain significance |
| rs144505423 | 1:118,483,784 | G/A | — | uncertain significance |
| rs765176394 | 1:118,485,134 | G/A | — | uncertain significance |
| rs1055806540 | 1:118,485,147 | A/G | — | uncertain significance |
| rs530007384 | 1:118,485,151 | A/G | — | uncertain significance |
| rs771302709 | 1:118,486,153 | T/C | — | uncertain significance |
| rs773567560 | 1:118,486,164 | C/T | — | uncertain significance |
| rs200959855 | 1:118,486,212 | C/G | — | uncertain significance |
| rs748137264 | 1:118,488,728 | C/T | — | uncertain significance |
| rs2525816151 | 1:118,488,731 | A/C | — | uncertain significance |
| rs2525816243 | 1:118,488,768 | T/A | — | uncertain significance |
| rs1266628635 | 1:118,491,079 | A/G | — | likely benign |
| rs1178116128 | 1:118,491,086 | C/G | — | uncertain significance |
| rs147807163 | 1:118,492,432 | T/C | — | uncertain significance |
| rs1224137710 | 1:118,492,659 | A/T | — | uncertain significance |
| rs769228463 | 1:118,492,703 | G/A | — | uncertain significance |
| rs2525825465 | 1:118,492,730 | A/G | — | uncertain significance |
| rs760784329 | 1:118,492,739 | G/T | — | uncertain significance |
| rs780951887 | 1:118,493,496 | T/C | — | uncertain significance |
| rs955865630 | 1:118,493,503 | A/C | — | uncertain significance |
| rs755664464 | 1:118,493,512 | A/T | — | uncertain significance |
| rs573261991 | 1:118,494,626 | G/A | — | uncertain significance |
| rs770636349 | 1:118,495,006 | A/G | — | uncertain significance |
| rs532257474 | 1:118,496,563 | C/G | — | — |
| rs4658973 | 1:118,499,054 | T/G | intron variant | — |
| rs369554244 | 1:118,499,714 | T/C | — | uncertain significance |
| rs200970120 | 1:118,501,561 | C/A | — | uncertain significance |
| rs748019710 | 1:118,501,564 | A/G | — | uncertain significance |
| rs777434802 | 1:118,501,576 | G/A | — | uncertain significance |
| rs1266195526 | 1:118,501,620 | A/C | — | uncertain significance |
| rs373860081 | 1:118,501,929 | C/A | — | uncertain significance |
| rs768211246 | 1:118,501,966 | G/A | — | uncertain significance |
| rs2525935826 | 1:118,501,975 | A/G | — | uncertain significance |
| rs137952009 | 1:118,501,976 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.