KIAA0232
KIAA0232
Summary
Predicted to enable ATP binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants77 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs538581873 | 4:6,803,992 | T/C | — | — |
| rs2549122117 | 4:6,826,197 | C/T | — | uncertain significance |
| rs764980426 | 4:6,826,205 | G/T | — | uncertain significance |
| rs111811307 | 4:6,826,228 | C/G | — | likely benign |
| rs2549122444 | 4:6,826,338 | A/T | — | uncertain significance |
| rs116723815 | 4:6,833,280 | G/C | intron variant | — |
| rs2549163660 | 4:6,843,822 | A/C | — | uncertain significance |
| rs199993317 | 4:6,843,884 | A/T | — | uncertain significance |
| rs188475539 | 4:6,843,931 | A/G | — | likely benign |
| rs35294480 | 4:6,857,840 | C/T | regulatory region variant | — |
| rs1476863445 | 4:6,860,178 | G/A | — | uncertain significance |
| rs752186773 | 4:6,862,716 | T/C | — | uncertain significance |
| rs757974831 | 4:6,862,726 | C/G | — | uncertain significance |
| rs774559773 | 4:6,862,795 | G/A | — | uncertain significance |
| rs2549206263 | 4:6,862,876 | A/C | — | uncertain significance |
| rs1342714319 | 4:6,862,888 | G/A | — | uncertain significance |
| rs750253473 | 4:6,862,929 | C/A | — | uncertain significance |
| rs374592929 | 4:6,863,092 | G/A | — | uncertain significance |
| rs367656934 | 4:6,863,124 | G/A | — | uncertain significance |
| rs370100944 | 4:6,863,151 | A/T | — | uncertain significance |
| rs776448878 | 4:6,863,155 | G/A | — | uncertain significance |
| rs765215228 | 4:6,863,166 | A/G | — | uncertain significance |
| rs758409390 | 4:6,863,185 | T/G | — | uncertain significance |
| rs144821735 | 4:6,863,215 | C/T | — | likely benign |
| rs1415202038 | 4:6,863,277 | A/C | — | uncertain significance |
| rs201585791 | 4:6,863,288 | C/A | — | uncertain significance |
| rs755549180 | 4:6,863,328 | A/G | — | uncertain significance |
| rs1352913283 | 4:6,863,533 | C/T | — | uncertain significance |
| rs1275716804 | 4:6,863,546 | G/C | — | uncertain significance |
| rs1196721394 | 4:6,863,605 | A/G | — | uncertain significance |
| rs376769124 | 4:6,863,614 | A/T | — | uncertain significance |
| rs2549209650 | 4:6,863,628 | A/G | — | uncertain significance |
| rs73796359 | 4:6,863,742 | A/G | — | likely benign |
| rs754626245 | 4:6,863,820 | A/G | — | uncertain significance |
| rs1335997262 | 4:6,863,833 | G/A | — | uncertain significance |
| rs199745129 | 4:6,863,866 | A/G | — | uncertain significance |
| rs758972656 | 4:6,863,985 | C/T | — | uncertain significance |
| rs557484440 | 4:6,864,001 | A/T | — | uncertain significance |
| rs187923587 | 4:6,864,022 | T/C | — | likely benign |
| rs780999317 | 4:6,864,025 | A/G | — | uncertain significance |
| rs2549212210 | 4:6,864,072 | T/C | — | uncertain significance |
| rs767295030 | 4:6,864,148 | T/C | — | uncertain significance |
| rs2549212809 | 4:6,864,211 | A/T | — | uncertain significance |
| rs1720945009 | 4:6,864,462 | A/G | — | uncertain significance |
| rs374904040 | 4:6,864,480 | G/A | — | uncertain significance |
| rs2549214765 | 4:6,864,520 | A/C | — | likely benign |
| rs200779052 | 4:6,864,556 | A/C | — | uncertain significance |
| rs746490506 | 4:6,864,664 | C/T | — | uncertain significance |
| rs144840805 | 4:6,864,690 | T/C | — | benign |
| rs1720964543 | 4:6,864,745 | G/A | — | likely benign |
| rs768776366 | 4:6,864,811 | G/A | — | uncertain significance |
| rs200090538 | 4:6,864,814 | A/G | — | uncertain significance |
| rs1373245948 | 4:6,864,832 | G/T | — | uncertain significance |
| rs2549216611 | 4:6,864,849 | C/A | — | uncertain significance |
| rs369997653 | 4:6,864,864 | G/A | — | uncertain significance |
| rs372990475 | 4:6,864,882 | G/A | — | uncertain significance |
| rs749054027 | 4:6,864,887 | C/A | — | uncertain significance |
| rs371024458 | 4:6,864,997 | C/G | — | uncertain significance |
| rs770975807 | 4:6,865,045 | G/A | — | uncertain significance |
| rs73796360 | 4:6,865,058 | T/C | — | benign |
| rs758153786 | 4:6,865,089 | G/A | — | uncertain significance |
| rs978008306 | 4:6,865,128 | A/G | — | uncertain significance |
| rs2549218052 | 4:6,865,150 | C/G | — | uncertain significance |
| rs780512122 | 4:6,865,287 | C/T | — | uncertain significance |
| rs377131932 | 4:6,865,332 | A/G | — | uncertain significance |
| rs371014807 | 4:6,865,423 | G/A | — | uncertain significance |
| rs116439703 | 4:6,865,521 | T/C | — | benign |
| rs16839403 | 4:6,865,569 | T/C | — | benign |
| rs1560204942 | 4:6,865,736 | G/C | — | uncertain significance |
| rs146753584 | 4:6,865,797 | T/G | — | uncertain significance |
| rs2549221659 | 4:6,865,873 | A/T | — | uncertain significance |
| rs765728942 | 4:6,873,307 | G/C | — | uncertain significance |
| rs149493190 | 4:6,882,580 | C/T | — | benign |
| rs372295449 | 4:6,882,581 | G/A | — | uncertain significance |
| rs1269878388 | 4:6,882,637 | G/A | — | uncertain significance |
| rs943713334 | 4:6,882,671 | T/C | — | uncertain significance |
| rs372985624 | 4:6,882,680 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.