CRACDL
CRACD like
Known Variants77 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1703720845 | 2:99,411,077 | G/A | — | uncertain significance |
| rs1703810864 | 2:99,412,631 | A/G | — | likely benign |
| rs73962467 | 2:99,412,654 | C/T | — | benign |
| rs368332570 | 2:99,412,655 | G/A | — | uncertain significance |
| rs750928579 | 2:99,412,664 | C/G | — | uncertain significance |
| rs771733695 | 2:99,412,695 | G/T | — | uncertain significance |
| rs1703818599 | 2:99,412,717 | T/C | — | uncertain significance |
| rs2104391011 | 2:99,412,725 | C/G | — | uncertain significance |
| rs79749347 | 2:99,413,825 | G/A | — | benign |
| rs201196594 | 2:99,413,866 | G/A | — | uncertain significance |
| rs768252754 | 2:99,413,925 | C/A | — | uncertain significance |
| rs376576235 | 2:99,413,928 | G/A | — | uncertain significance |
| rs371156943 | 2:99,413,996 | C/A | — | uncertain significance |
| rs758111492 | 2:99,438,331 | C/T | — | likely benign |
| rs2467615962 | 2:99,438,362 | C/T | — | uncertain significance |
| rs150915151 | 2:99,438,421 | G/A | — | uncertain significance |
| rs955437607 | 2:99,438,441 | C/G | — | uncertain significance |
| rs775371612 | 2:99,438,484 | C/T | — | uncertain significance |
| rs373813701 | 2:99,438,485 | G/A | — | uncertain significance |
| rs1332100784 | 2:99,438,494 | C/A | — | uncertain significance |
| rs779381800 | 2:99,438,536 | G/C | — | uncertain significance |
| rs1044574093 | 2:99,438,585 | C/G | — | uncertain significance |
| rs200427787 | 2:99,438,624 | C/G | — | uncertain significance |
| rs778127726 | 2:99,438,671 | T/A | — | uncertain significance |
| rs558018207 | 2:99,438,695 | G/A | — | uncertain significance |
| rs1430105774 | 2:99,438,701 | T/C | — | uncertain significance |
| rs1167720040 | 2:99,438,704 | C/T | — | uncertain significance |
| rs571671010 | 2:99,438,733 | G/T | — | uncertain significance |
| rs749600144 | 2:99,438,740 | G/C | — | uncertain significance |
| rs1705083485 | 2:99,438,744 | T/G | — | uncertain significance |
| rs2467621269 | 2:99,438,755 | G/A | — | uncertain significance |
| rs756392778 | 2:99,438,758 | C/T | — | uncertain significance |
| rs557788758 | 2:99,438,784 | C/A | — | uncertain significance |
| rs1412652922 | 2:99,438,853 | C/T | — | likely benign |
| rs770753823 | 2:99,438,864 | G/C | — | uncertain significance |
| rs1277251656 | 2:99,438,894 | G/C | — | uncertain significance |
| rs750553841 | 2:99,439,012 | G/C | — | uncertain significance |
| rs1051488673 | 2:99,439,015 | A/T | — | uncertain significance |
| rs962357462 | 2:99,439,027 | C/A | — | uncertain significance |
| rs1395269465 | 2:99,439,067 | G/T | — | uncertain significance |
| rs1575348601 | 2:99,439,105 | C/T | — | likely benign |
| rs2467627105 | 2:99,439,124 | C/T | — | uncertain significance |
| rs1179392406 | 2:99,439,279 | G/C | — | uncertain significance |
| rs1208965154 | 2:99,439,313 | C/G | — | uncertain significance |
| rs377327569 | 2:99,439,331 | C/T | — | uncertain significance |
| rs367857987 | 2:99,439,355 | C/T | — | uncertain significance |
| rs774059631 | 2:99,439,375 | G/C | — | uncertain significance |
| rs781258791 | 2:99,439,378 | G/A | — | uncertain significance |
| rs1377857671 | 2:99,439,379 | G/A | — | uncertain significance |
| rs755683722 | 2:99,439,393 | T/C | — | uncertain significance |
| rs779624709 | 2:99,439,469 | C/T | — | uncertain significance |
| rs1430348754 | 2:99,439,511 | C/G | — | uncertain significance |
| rs748390102 | 2:99,439,612 | G/T | — | uncertain significance |
| rs891555064 | 2:99,439,654 | G/T | — | uncertain significance |
| rs2467635671 | 2:99,439,667 | G/A | — | uncertain significance |
| rs2467635701 | 2:99,439,669 | G/T | — | uncertain significance |
| rs2467636004 | 2:99,439,688 | G/C | — | uncertain significance |
| rs779205825 | 2:99,439,696 | G/A | — | uncertain significance |
| rs925200590 | 2:99,439,703 | C/T | — | uncertain significance |
| rs773278161 | 2:99,439,742 | G/A | — | uncertain significance |
| rs1356326704 | 2:99,439,766 | C/T | — | uncertain significance |
| rs372620989 | 2:99,439,883 | C/T | — | uncertain significance |
| rs777863533 | 2:99,439,906 | C/T | — | uncertain significance |
| rs1347644212 | 2:99,439,949 | C/T | — | uncertain significance |
| rs374696900 | 2:99,439,955 | C/T | — | uncertain significance |
| rs538995720 | 2:99,441,815 | G/A | — | — |
| rs990740380 | 2:99,443,471 | G/C | — | uncertain significance |
| rs184848302 | 2:99,443,583 | C/T | — | uncertain significance |
| rs550266039 | 2:99,448,912 | G/A | — | uncertain significance |
| rs1705585018 | 2:99,448,939 | G/C | — | uncertain significance |
| rs2467683973 | 2:99,448,951 | T/C | — | uncertain significance |
| rs1474745104 | 2:99,448,954 | T/G | — | uncertain significance |
| rs2467742872 | 2:99,463,208 | C/T | — | uncertain significance |
| rs967032367 | 2:99,463,230 | G/A | — | uncertain significance |
| rs6733011 | 2:99,465,502 | A/G | intron variant | — |
| rs12712040 | 2:99,513,416 | G/C | intron variant | — |
| rs575488433 | 2:99,547,092 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.