WDR27
WD repeat domain 27
Summary
This gene encodes a protein with multiple WD repeats. Proteins with these repeats may form scaffolds for protein-protein interaction and play key roles in cell signalling. Alternative splicing results in multiple transcript variants, but the full-length structure of some of these variants cannot be determined. [provided by RefSeq, Nov 2015]
Known Variants74 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs147527958 | 6:169,888,502 | C/T | intron variant | — |
| rs542047810 | 6:169,895,859 | T/C | — | — |
| rs3734905 | 6:169,958,982 | G/A | regulatory region variant | — |
| rs10945439 | 6:169,972,627 | G/A | — | benign |
| rs9396979 | 6:169,982,242 | G/C | — | — |
| rs780259952 | 6:169,982,934 | G/T | — | uncertain significance |
| rs377595185 | 6:169,982,979 | G/A | — | uncertain significance |
| rs374609796 | 6:169,983,018 | C/G | — | uncertain significance |
| rs751385652 | 6:170,002,319 | C/T | — | uncertain significance |
| rs748691978 | 6:170,002,341 | C/T | — | uncertain significance |
| rs773704528 | 6:170,002,356 | G/A | — | uncertain significance |
| rs201412987 | 6:170,002,365 | C/T | — | uncertain significance |
| rs41265373 | 6:170,002,391 | G/A | — | uncertain significance |
| rs377120387 | 6:170,002,409 | C/T | — | uncertain significance |
| rs149946921 | 6:170,002,413 | C/G | — | uncertain significance |
| rs1461672153 | 6:170,013,751 | C/A | — | uncertain significance |
| rs376239890 | 6:170,033,071 | C/T | — | uncertain significance |
| rs370579184 | 6:170,033,072 | G/A | — | uncertain significance |
| rs200076349 | 6:170,033,108 | C/T | — | uncertain significance |
| rs752753328 | 6:170,033,113 | T/C | — | uncertain significance |
| rs2536179567 | 6:170,033,116 | A/G | — | uncertain significance |
| rs201723267 | 6:170,034,538 | T/C | — | uncertain significance |
| rs777651924 | 6:170,034,560 | T/C | — | likely benign |
| rs769264674 | 6:170,034,581 | A/G | — | likely benign |
| rs376587997 | 6:170,036,494 | A/G | — | uncertain significance |
| rs202036897 | 6:170,036,506 | A/C | — | uncertain significance |
| rs763944673 | 6:170,036,524 | C/A | — | uncertain significance |
| rs2536225005 | 6:170,036,541 | A/T | — | uncertain significance |
| rs369074175 | 6:170,038,646 | C/T | — | uncertain significance |
| rs202243345 | 6:170,038,703 | G/C | — | uncertain significance |
| rs200680182 | 6:170,038,749 | G/T | — | uncertain significance |
| rs7744717 | 6:170,049,350 | C/A | — | uncertain significance |
| rs765521537 | 6:170,052,033 | C/G | — | uncertain significance |
| rs747934669 | 6:170,052,063 | T/C | — | uncertain significance |
| rs41265379 | 6:170,052,078 | G/A | — | uncertain significance |
| rs371086301 | 6:170,052,093 | C/T | — | uncertain significance |
| rs371902451 | 6:170,058,395 | T/C | — | uncertain significance |
| rs373742623 | 6:170,058,406 | C/G | — | uncertain significance |
| rs1304247389 | 6:170,058,426 | A/G | — | uncertain significance |
| rs1187525478 | 6:170,059,239 | G/A | — | uncertain significance |
| rs371337921 | 6:170,059,240 | C/T | — | uncertain significance |
| rs567926770 | 6:170,059,260 | A/G | — | uncertain significance |
| rs763294437 | 6:170,059,261 | C/T | — | uncertain significance |
| rs1200241380 | 6:170,059,273 | C/T | — | uncertain significance |
| rs201212947 | 6:170,059,279 | A/G | — | uncertain significance |
| rs754838684 | 6:170,059,284 | G/A | — | uncertain significance |
| rs200546538 | 6:170,059,563 | C/T | — | uncertain significance |
| rs373414507 | 6:170,059,566 | T/C | — | likely benign |
| rs1222502112 | 6:170,060,818 | A/C | — | uncertain significance |
| rs375032783 | 6:170,060,840 | A/G | — | uncertain significance |
| rs201122874 | 6:170,060,843 | G/C | — | uncertain significance |
| rs1825849701 | 6:170,060,852 | C/T | — | uncertain significance |
| rs1220112093 | 6:170,062,490 | A/G | — | uncertain significance |
| rs2536645535 | 6:170,062,514 | C/T | — | uncertain significance |
| rs760715743 | 6:170,064,283 | A/T | — | uncertain significance |
| rs2536686749 | 6:170,064,300 | G/A | — | likely benign |
| rs148005563 | 6:170,064,333 | C/T | — | uncertain significance |
| rs373953626 | 6:170,064,345 | C/T | — | uncertain significance |
| rs200494024 | 6:170,064,346 | G/A | — | uncertain significance |
| rs760508495 | 6:170,065,599 | C/T | — | uncertain significance |
| rs199590890 | 6:170,068,109 | A/C | — | uncertain significance |
| rs180785216 | 6:170,068,151 | G/A | — | uncertain significance |
| rs185125982 | 6:170,068,178 | C/A | — | likely benign |
| rs780774419 | 6:170,068,229 | T/C | — | uncertain significance |
| rs375738312 | 6:170,068,277 | C/T | — | uncertain significance |
| rs749973330 | 6:170,070,696 | G/T | — | uncertain significance |
| rs778484287 | 6:170,070,772 | T/C | — | uncertain significance |
| rs2536845791 | 6:170,072,393 | T/C | — | uncertain significance |
| rs1200092713 | 6:170,072,411 | C/T | — | uncertain significance |
| rs4236177 | 6:170,073,543 | C/T | intron variant | — |
| rs543503307 | 6:170,084,874 | C/T | — | — |
| rs561673923 | 6:170,088,924 | G/A | — | uncertain significance |
| rs778024073 | 6:170,088,998 | T/A | — | uncertain significance |
| rs1562939740 | 6:170,089,048 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.