UNC93A
unc-93 homolog A
Summary
Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs73257132 | 6:167,690,244 | G/A | intron variant | — |
| rs374730365 | 6:167,705,003 | T/C | — | uncertain significance |
| rs776571748 | 6:167,708,032 | G/A | — | uncertain significance |
| rs369188282 | 6:167,708,042 | C/T | — | uncertain significance |
| rs1190916321 | 6:167,708,095 | C/G | — | uncertain significance |
| rs200753568 | 6:167,709,563 | G/A | — | uncertain significance |
| rs202053224 | 6:167,709,567 | C/T | — | uncertain significance |
| rs761935242 | 6:167,709,635 | C/T | — | uncertain significance |
| rs772148244 | 6:167,709,636 | G/A | — | likely benign |
| rs150440399 | 6:167,709,705 | G/A | — | likely benign |
| rs774391259 | 6:167,709,746 | C/A | — | uncertain significance |
| rs760694647 | 6:167,711,477 | T/G | — | uncertain significance |
| rs2533488227 | 6:167,711,495 | A/G | — | uncertain significance |
| rs753048382 | 6:167,711,531 | G/A | — | likely benign |
| rs2346119 | 6:167,712,621 | C/T | — | — |
| rs2346120 | 6:167,712,623 | C/A | — | — |
| rs12662820 | 6:167,715,738 | G/T | intron variant | — |
| rs12665714 | 6:167,715,771 | A/C | intron variant | — |
| rs34838751 | 6:167,717,440 | C/T | — | benign |
| rs145360877 | 6:167,717,457 | C/T | — | likely benign |
| rs550819069 | 6:167,717,458 | G/A | — | uncertain significance |
| rs140993385 | 6:167,717,469 | C/T | — | uncertain significance |
| rs2533510552 | 6:167,719,413 | C/G | — | uncertain significance |
| rs4708771 | 6:167,719,445 | G/T | — | uncertain significance |
| rs35854179 | 6:167,719,484 | G/A | — | benign |
| rs2533511141 | 6:167,719,500 | T/C | — | uncertain significance |
| rs376103334 | 6:167,719,503 | C/T | — | uncertain significance |
| rs144446179 | 6:167,719,513 | G/A | — | likely benign |
| rs61729547 | 6:167,721,268 | C/T | — | benign |
| rs368129820 | 6:167,721,270 | C/T | — | uncertain significance |
| rs758878977 | 6:167,721,273 | T/G | — | uncertain significance |
| rs1371579516 | 6:167,721,297 | C/T | — | uncertain significance |
| rs267600893 | 6:167,721,317 | C/T | — | uncertain significance |
| rs772759538 | 6:167,728,683 | G/C | — | uncertain significance |
| rs572198078 | 6:167,728,686 | G/A | — | uncertain significance |
| rs750381322 | 6:167,728,723 | A/G | — | uncertain significance |
| rs200775978 | 6:167,728,729 | G/A | — | uncertain significance |
| rs146482775 | 6:167,728,741 | C/T | — | uncertain significance |
| rs663606 | 6:167,728,774 | C/T | — | benign |
| rs9459921 | 6:167,728,775 | G/A | — | benign |
| rs112580447 | 6:167,728,784 | C/T | — | likely benign |
| rs1245201649 | 6:167,728,843 | G/A | — | uncertain significance |
| rs536332358 | 6:167,728,857 | G/A | — | uncertain significance |
| rs1370568839 | 6:167,728,866 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.