KIAA0825
KIAA0825
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs17376456 | 5:93,557,702 | A/G | intron variant | — |
| rs2434364 | 5:93,697,852 | C/G | — | — |
| rs62364586 | 5:93,720,171 | T/C | — | benign |
| rs776944748 | 5:93,721,994 | G/A | — | uncertain significance |
| rs72771666 | 5:93,722,036 | A/G | — | benign |
| rs763611790 | 5:93,722,049 | G/A | — | uncertain significance |
| rs29913 | 5:93,722,050 | G/T | — | benign |
| rs75413171 | 5:93,727,244 | T/C | — | benign |
| rs373480280 | 5:93,727,325 | A/C | — | likely benign |
| rs556550987 | 5:93,731,957 | C/A | — | uncertain significance |
| rs308207 | 5:93,731,985 | A/G | — | benign |
| rs185381772 | 5:93,732,089 | A/T | — | likely benign |
| rs2546614826 | 5:93,739,355 | C/A | — | uncertain significance |
| rs1026880655 | 5:93,752,998 | T/A | — | uncertain significance |
| rs29910 | 5:93,753,017 | C/T | — | benign |
| rs29909 | 5:93,753,060 | G/A | — | benign |
| rs777459977 | 5:93,775,768 | G/T | — | uncertain significance |
| rs180852937 | 5:93,798,142 | A/T | — | benign |
| rs956457873 | 5:93,798,165 | T/A | — | uncertain significance |
| rs191923841 | 5:93,798,252 | T/G | — | likely benign |
| rs201212314 | 5:93,800,617 | A/T | — | likely pathogenic |
| rs17379264 | 5:93,800,660 | C/T | — | benign |
| rs2546875840 | 5:93,800,679 | T/C | — | uncertain significance |
| rs759087301 | 5:93,800,758 | T/C | — | uncertain significance |
| rs192280399 | 5:93,805,705 | A/G | — | benign |
| rs114467120 | 5:93,807,200 | A/G | — | benign |
| rs79996980 | 5:93,807,265 | G/A | — | uncertain significance |
| rs374186567 | 5:93,809,166 | G/A | — | uncertain significance |
| rs6869388 | 5:93,810,208 | T/C | intron variant | — |
| rs77179804 | 5:93,812,816 | C/T | — | benign |
| rs10057902 | 5:93,812,885 | C/T | — | benign |
| rs143619655 | 5:93,820,470 | T/C | — | benign |
| rs77357740 | 5:93,820,568 | C/T | — | benign |
| rs149370841 | 5:93,855,954 | C/A | — | uncertain significance |
| rs768867502 | 5:93,855,997 | G/A | — | uncertain significance |
| rs148504794 | 5:93,856,145 | T/C | — | uncertain significance |
| rs143278447 | 5:93,856,225 | C/T | — | uncertain significance |
| rs2547098973 | 5:93,856,229 | T/C | — | uncertain significance |
| rs1768026365 | 5:93,856,480 | G/A | — | uncertain significance |
| rs766044682 | 5:93,856,582 | G/A | — | likely benign |
| rs1442358772 | 5:93,856,600 | T/C | — | uncertain significance |
| rs758127035 | 5:93,859,642 | T/C | — | uncertain significance |
| rs1227670867 | 5:93,859,757 | A/C | — | uncertain significance |
| rs147120237 | 5:93,859,772 | C/T | — | uncertain significance |
| rs2044909 | 5:93,859,799 | T/C | — | benign |
| rs758601966 | 5:93,872,731 | A/G | — | uncertain significance |
| rs1239940017 | 5:93,872,782 | A/G | — | pathogenic |
Gene information from NCBI Gene. Variant classifications from ClinVar.