KIAA1217
KIAA1217
Summary
Predicted to be involved in embryonic skeletal system development. Located in centrosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants126 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10828538 | 10:24,041,317 | A/T | intron variant | — |
| rs80167153 | 10:24,129,791 | T/A | intron variant | — |
| rs75058681 | 10:24,132,019 | A/G | intron variant | — |
| rs117321564 | 10:24,172,797 | C/T | intron variant | — |
| rs965547506 | 10:24,460,740 | C/T | — | — |
| rs11013962 | 10:24,495,586 | A/T | — | — |
| rs2067761081 | 10:24,498,181 | G/A | — | uncertain significance |
| rs577526247 | 10:24,508,578 | G/A | — | uncertain significance |
| rs767704495 | 10:24,508,672 | T/A | — | uncertain significance |
| rs184688700 | 10:24,508,786 | A/G | — | uncertain significance |
| rs754497667 | 10:24,508,831 | G/A | — | uncertain significance |
| rs11014002 | 10:24,564,653 | C/T | coding sequence variant | — |
| rs16924573 | 10:24,604,893 | G/A | intron variant | — |
| rs2484873 | 10:24,634,956 | A/G | intron variant | — |
| rs758902169 | 10:24,669,910 | C/T | — | uncertain significance |
| rs531923158 | 10:24,669,946 | C/T | — | uncertain significance |
| rs3858217 | 10:24,690,604 | G/C | intron variant | — |
| rs771938876 | 10:24,721,941 | T/C | — | uncertain significance |
| rs201441351 | 10:24,722,074 | A/G | — | uncertain significance |
| rs61735610 | 10:24,727,317 | A/G | — | uncertain significance |
| rs754581453 | 10:24,727,376 | C/T | — | uncertain significance |
| rs767627092 | 10:24,762,179 | C/A | — | uncertain significance |
| rs771590028 | 10:24,762,236 | C/T | — | uncertain significance |
| rs2542141013 | 10:24,762,310 | G/A | — | uncertain significance |
| rs774456939 | 10:24,762,406 | G/A | — | uncertain significance |
| rs1312932343 | 10:24,762,413 | T/C | — | uncertain significance |
| rs754183744 | 10:24,762,445 | A/T | — | uncertain significance |
| rs141833772 | 10:24,762,667 | C/G | — | uncertain significance |
| rs750065477 | 10:24,762,725 | C/G | — | uncertain significance |
| rs139061769 | 10:24,762,760 | A/G | — | likely benign |
| rs150047311 | 10:24,762,790 | G/A | — | uncertain significance |
| rs1429938025 | 10:24,762,817 | C/T | — | uncertain significance |
| rs201854162 | 10:24,762,860 | C/T | — | uncertain significance |
| rs772585153 | 10:24,762,884 | G/A | — | uncertain significance |
| rs368075111 | 10:24,762,889 | G/A | — | likely benign |
| rs61735604 | 10:24,762,892 | G/A | — | benign |
| rs563623304 | 10:24,762,959 | C/T | — | uncertain significance |
| rs148941784 | 10:24,783,527 | C/T | — | uncertain significance |
| rs2543140461 | 10:24,790,326 | G/C | — | uncertain significance |
| rs2543140648 | 10:24,790,334 | A/T | — | uncertain significance |
| rs758247332 | 10:24,790,430 | G/A | — | uncertain significance |
| rs199737801 | 10:24,790,434 | C/T | — | uncertain significance |
| rs1409791438 | 10:24,790,444 | G/T | — | uncertain significance |
| rs1335434800 | 10:24,790,468 | G/C | — | uncertain significance |
| rs187214051 | 10:24,802,192 | A/G | — | uncertain significance |
| rs745471937 | 10:24,802,216 | T/A | — | uncertain significance |
| rs571225556 | 10:24,802,230 | G/A | — | uncertain significance |
| rs753924454 | 10:24,802,297 | G/A | — | uncertain significance |
| rs536051127 | 10:24,802,350 | G/A | — | likely benign |
| rs761928869 | 10:24,809,125 | G/A | — | uncertain significance |
| rs755318277 | 10:24,809,137 | G/T | — | uncertain significance |
| rs374750962 | 10:24,810,819 | G/A | — | uncertain significance |
| rs138527418 | 10:24,813,285 | C/T | — | likely benign |
| rs113571639 | 10:24,813,297 | C/T | — | benign |
| rs141384251 | 10:24,813,298 | G/A | — | uncertain significance |
| rs535623524 | 10:24,813,369 | C/T | — | likely benign |
| rs146210961 | 10:24,813,373 | G/A | — | likely benign |
| rs369719080 | 10:24,813,406 | G/A | — | uncertain significance |
| rs145932195 | 10:24,813,443 | T/C | — | likely benign |
| rs147898647 | 10:24,813,493 | T/C | — | uncertain significance |
| rs141672009 | 10:24,813,535 | G/C | — | uncertain significance |
| rs147067816 | 10:24,813,540 | C/G | — | uncertain significance |
| rs2543990127 | 10:24,813,563 | C/T | — | likely benign |
| rs2071813987 | 10:24,813,599 | C/A | — | uncertain significance |
| rs1236824380 | 10:24,816,887 | A/G | — | uncertain significance |
| rs375000847 | 10:24,816,899 | A/G | — | uncertain significance |
| rs2544111431 | 10:24,816,905 | A/T | — | uncertain significance |
| rs376587403 | 10:24,816,989 | C/T | — | uncertain significance |
| rs148599992 | 10:24,817,027 | G/T | — | likely benign |
| rs551634178 | 10:24,820,801 | G/T | — | uncertain significance |
| rs267602448 | 10:24,820,833 | C/T | — | uncertain significance |
| rs755218204 | 10:24,820,834 | G/T | — | uncertain significance |
| rs745318950 | 10:24,820,855 | C/T | — | uncertain significance |
| rs371056850 | 10:24,820,917 | G/A | — | uncertain significance |
| rs780736647 | 10:24,822,014 | G/T | — | uncertain significance |
| rs747791742 | 10:24,822,015 | C/T | — | uncertain significance |
| rs757566686 | 10:24,822,071 | G/C | — | uncertain significance |
| rs374052578 | 10:24,822,090 | C/T | — | benign |
| rs1433034856 | 10:24,822,102 | C/T | — | uncertain significance |
| rs201090723 | 10:24,822,104 | T/G | — | uncertain significance |
| rs2073383555 | 10:24,822,134 | G/A | — | uncertain significance |
| rs145406190 | 10:24,825,761 | G/A | — | uncertain significance |
| rs368933412 | 10:24,825,768 | C/G | — | uncertain significance |
| rs2544457765 | 10:24,825,781 | G/A | — | uncertain significance |
| rs753438365 | 10:24,825,789 | G/T | — | uncertain significance |
| rs149136297 | 10:24,831,685 | A/G | — | likely benign |
| rs59421477 | 10:24,831,846 | C/T | — | benign |
| rs1208321933 | 10:24,831,990 | C/T | — | uncertain significance |
| rs150113984 | 10:24,832,098 | C/T | — | uncertain significance |
| rs2544701630 | 10:24,832,100 | C/A | — | likely benign |
| rs773032397 | 10:24,832,109 | G/A | — | uncertain significance |
| rs774541605 | 10:24,832,139 | A/G | — | uncertain significance |
| rs369723065 | 10:24,832,170 | G/T | — | uncertain significance |
| rs142383483 | 10:24,832,224 | C/G | — | benign |
| rs775755366 | 10:24,832,379 | G/T | — | uncertain significance |
| rs2544712713 | 10:24,832,407 | T/C | — | uncertain significance |
| rs147986443 | 10:24,832,430 | A/G | — | likely benign |
| rs200193590 | 10:24,832,447 | C/T | — | likely benign |
| rs61734877 | 10:24,832,467 | C/A | — | uncertain significance |
| rs140457046 | 10:24,832,540 | C/T | — | likely benign |
Showing 100 of 126 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.