ANKUB1
ankyrin repeat and ubiquitin domain containing 1
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200339770 | 3:149,479,284 | T/C | — | uncertain significance |
| rs910906428 | 3:149,479,312 | C/G | — | uncertain significance |
| rs755269424 | 3:149,479,314 | C/T | — | uncertain significance |
| rs189184582 | 3:149,484,962 | T/C | — | uncertain significance |
| rs986794872 | 3:149,484,968 | G/A | — | uncertain significance |
| rs1311592241 | 3:149,485,064 | G/T | — | uncertain significance |
| rs1483307791 | 3:149,485,068 | G/A | — | uncertain significance |
| rs1174585383 | 3:149,485,100 | G/A | — | uncertain significance |
| rs189568065 | 3:149,485,104 | C/T | — | uncertain significance |
| rs1717073448 | 3:149,485,107 | G/C | — | uncertain significance |
| rs2472979406 | 3:149,485,191 | G/C | — | uncertain significance |
| rs1166723161 | 3:149,485,329 | C/T | — | uncertain significance |
| rs923755969 | 3:149,485,356 | C/A | — | uncertain significance |
| rs1273166145 | 3:149,485,385 | G/A | — | uncertain significance |
| rs2472980571 | 3:149,485,446 | C/G | — | likely benign |
| rs536450401 | 3:149,485,448 | C/T | — | uncertain significance |
| rs1228176647 | 3:149,485,473 | G/A | — | uncertain significance |
| rs1472937646 | 3:149,485,496 | T/G | — | uncertain significance |
| rs369106386 | 3:149,485,521 | T/C | — | uncertain significance |
| rs565959832 | 3:149,485,533 | T/G | — | uncertain significance |
| rs1263375296 | 3:149,485,555 | C/A | — | uncertain significance |
| rs1481128803 | 3:149,485,623 | T/C | — | uncertain significance |
| rs377486050 | 3:149,485,625 | T/C | — | uncertain significance |
| rs1717123296 | 3:149,485,629 | C/T | — | uncertain significance |
| rs999593020 | 3:149,485,707 | C/T | — | uncertain significance |
| rs568985802 | 3:149,485,782 | C/T | — | uncertain significance |
| rs371783801 | 3:149,488,377 | C/T | — | uncertain significance |
| rs900457730 | 3:149,488,387 | T/C | — | uncertain significance |
| rs1387779723 | 3:149,488,441 | C/T | — | uncertain significance |
| rs62622807 | 3:149,498,097 | T/G | — | uncertain significance |
| rs746634770 | 3:149,498,226 | G/T | — | uncertain significance |
| rs1718325844 | 3:149,508,617 | A/G | — | uncertain significance |
| rs1289549958 | 3:149,508,624 | A/C | — | uncertain significance |
| rs1044353589 | 3:149,510,096 | C/T | — | uncertain significance |
| rs577348720 | 3:149,510,138 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.