KIAA0930
KIAA0930
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs759747238 | 22:45,593,701 | C/T | — | uncertain significance |
| rs868065352 | 22:45,593,778 | C/T | — | uncertain significance |
| rs2147734937 | 22:45,595,796 | C/T | — | likely pathogenic |
| rs2147734941 | 22:45,595,798 | G/A | — | conflicting classifications of pathogenicity |
| rs2147734951 | 22:45,595,804 | G/A | — | likely pathogenic |
| rs768264629 | 22:45,595,826 | G/A | — | uncertain significance |
| rs376273127 | 22:45,595,831 | C/T | — | uncertain significance |
| rs766893628 | 22:45,595,840 | T/C | — | uncertain significance |
| rs1456173544 | 22:45,595,870 | G/C | — | uncertain significance |
| rs1831567641 | 22:45,598,885 | G/A | — | uncertain significance |
| rs373895809 | 22:45,599,033 | C/T | — | uncertain significance |
| rs751295257 | 22:45,599,053 | C/T | — | uncertain significance |
| rs138154810 | 22:45,599,808 | C/T | — | uncertain significance |
| rs202199648 | 22:45,601,715 | C/T | — | uncertain significance |
| rs949177414 | 22:45,601,718 | T/C | — | uncertain significance |
| rs1463975403 | 22:45,601,756 | C/T | — | uncertain significance |
| rs764509236 | 22:45,607,854 | C/T | — | likely benign |
| rs56194783 | 22:45,607,855 | G/A | — | benign |
| rs575606111 | 22:45,607,884 | G/A | — | uncertain significance |
| rs1325271672 | 22:45,607,971 | G/A | — | uncertain significance |
| rs770782781 | 22:45,608,163 | A/G | — | uncertain significance |
| rs373339760 | 22:45,608,172 | G/A | — | uncertain significance |
| rs2518073122 | 22:45,608,184 | G/A | — | uncertain significance |
| rs150665432 | 22:45,608,215 | G/A | — | likely benign |
| rs5766574 | 22:45,629,198 | G/A | intron variant | — |
| rs11704685 | 22:45,632,109 | G/A | regulatory region variant | — |
| rs5766582 | 22:45,632,528 | C/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.