KIAA1549L
KIAA1549 like
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants110 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2753411 | 11:33,405,001 | A/T | regulatory region variant | — |
| rs183878278 | 11:33,564,038 | T/C | — | uncertain significance |
| rs761592361 | 11:33,564,100 | A/G | — | likely benign |
| rs371587246 | 11:33,564,124 | T/C | — | uncertain significance |
| rs373682730 | 11:33,564,146 | G/T | — | uncertain significance |
| rs769507031 | 11:33,564,170 | C/T | — | likely benign |
| rs527617353 | 11:33,564,173 | C/T | — | uncertain significance |
| rs2494748147 | 11:33,564,268 | C/G | — | uncertain significance |
| rs774184020 | 11:33,564,310 | G/A | — | uncertain significance |
| rs199578357 | 11:33,564,350 | A/G | — | uncertain significance |
| rs777193085 | 11:33,564,374 | A/G | — | uncertain significance |
| rs896030665 | 11:33,564,404 | C/T | — | uncertain significance |
| rs199813071 | 11:33,564,565 | C/T | — | uncertain significance |
| rs753379765 | 11:33,564,622 | C/T | — | uncertain significance |
| rs758405482 | 11:33,564,863 | C/T | — | uncertain significance |
| rs200017530 | 11:33,564,982 | C/T | — | uncertain significance |
| rs375294941 | 11:33,565,001 | C/G | — | uncertain significance |
| rs886870651 | 11:33,565,069 | G/A | — | uncertain significance |
| rs779465273 | 11:33,565,110 | A/C | — | uncertain significance |
| rs377701052 | 11:33,565,114 | G/T | — | uncertain significance |
| rs1565176802 | 11:33,565,163 | G/A | — | uncertain significance |
| rs200940153 | 11:33,565,178 | C/T | — | uncertain significance |
| rs1345413075 | 11:33,565,214 | C/A | — | uncertain significance |
| rs779669457 | 11:33,565,248 | A/G | — | uncertain significance |
| rs768134400 | 11:33,565,253 | G/C | — | uncertain significance |
| rs760798549 | 11:33,565,307 | G/T | — | uncertain significance |
| rs376512899 | 11:33,565,325 | C/T | — | uncertain significance |
| rs79216682 | 11:33,565,338 | T/C | — | benign |
| rs201621980 | 11:33,565,450 | A/G | — | uncertain significance |
| rs749010660 | 11:33,565,489 | A/G | — | likely benign |
| rs751888595 | 11:33,565,523 | G/A | — | uncertain significance |
| rs377249336 | 11:33,565,736 | A/G | — | uncertain significance |
| rs756839939 | 11:33,565,757 | C/G | — | uncertain significance |
| rs201050628 | 11:33,565,810 | A/G | — | uncertain significance |
| rs776064386 | 11:33,565,852 | C/T | — | uncertain significance |
| rs781582126 | 11:33,566,313 | C/T | — | likely benign |
| rs371851319 | 11:33,566,415 | A/G | — | uncertain significance |
| rs1854185601 | 11:33,566,463 | G/T | — | uncertain significance |
| rs1854187186 | 11:33,566,488 | A/C | — | uncertain significance |
| rs199569336 | 11:33,566,539 | C/G | — | likely benign |
| rs370422408 | 11:33,566,727 | C/T | — | uncertain significance |
| rs1854205503 | 11:33,566,771 | A/G | — | uncertain significance |
| rs373566420 | 11:33,566,795 | C/T | — | uncertain significance |
| rs183458242 | 11:33,566,806 | A/C | — | likely benign |
| rs1375400915 | 11:33,569,360 | A/G | — | uncertain significance |
| rs776240568 | 11:33,569,366 | G/A | — | uncertain significance |
| rs2133197804 | 11:33,572,622 | G/A | — | uncertain significance |
| rs2494791156 | 11:33,573,660 | A/C | — | uncertain significance |
| rs368484915 | 11:33,573,675 | C/T | — | uncertain significance |
| rs550449937 | 11:33,573,726 | A/G | — | uncertain significance |
| rs2494791978 | 11:33,573,775 | C/G | — | uncertain significance |
| rs373132227 | 11:33,581,379 | G/A | — | uncertain significance |
| rs367564819 | 11:33,583,228 | A/C | — | uncertain significance |
| rs550171641 | 11:33,585,744 | C/T | — | — |
| rs10437629 | 11:33,588,210 | A/G | intron variant | — |
| rs139772715 | 11:33,596,277 | G/A | — | likely benign |
| rs61735318 | 11:33,596,316 | C/T | — | benign |
| rs760625170 | 11:33,596,336 | C/T | — | uncertain significance |
| rs2494963726 | 11:33,612,864 | A/T | — | uncertain significance |
| rs908037147 | 11:33,612,920 | G/T | — | uncertain significance |
| rs375058535 | 11:33,612,954 | G/A | — | uncertain significance |
| rs377520713 | 11:33,628,229 | A/G | — | likely benign |
| rs140833560 | 11:33,628,232 | C/T | — | uncertain significance |
| rs375618485 | 11:33,628,243 | G/A | — | uncertain significance |
| rs1374392540 | 11:33,628,283 | T/C | — | uncertain significance |
| rs199851808 | 11:33,628,306 | C/T | — | uncertain significance |
| rs1421739831 | 11:33,628,349 | C/T | — | uncertain significance |
| rs752241863 | 11:33,628,363 | G/A | — | uncertain significance |
| rs1419044157 | 11:33,631,305 | C/T | — | uncertain significance |
| rs756947000 | 11:33,631,338 | G/A | — | uncertain significance |
| rs778487707 | 11:33,631,349 | C/T | — | uncertain significance |
| rs554792436 | 11:33,631,376 | T/C | — | uncertain significance |
| rs373216368 | 11:33,631,398 | C/T | — | uncertain significance |
| rs754959729 | 11:33,631,443 | C/T | — | uncertain significance |
| rs2495047329 | 11:33,631,466 | G/A | — | uncertain significance |
| rs2495047651 | 11:33,631,500 | A/C | — | uncertain significance |
| rs780296532 | 11:33,640,105 | G/A | — | uncertain significance |
| rs759144156 | 11:33,640,168 | G/A | — | uncertain significance |
| rs369880308 | 11:33,667,283 | C/T | — | uncertain significance |
| rs775563655 | 11:33,667,418 | C/T | — | uncertain significance |
| rs61735321 | 11:33,667,424 | G/A | — | benign |
| rs373633010 | 11:33,667,433 | C/T | — | uncertain significance |
| rs370779771 | 11:33,667,470 | C/T | — | uncertain significance |
| rs776673634 | 11:33,667,493 | G/A | — | uncertain significance |
| rs1038914142 | 11:33,667,512 | G/A | — | uncertain significance |
| rs767101653 | 11:33,667,523 | G/A | — | uncertain significance |
| rs202016116 | 11:33,667,556 | A/G | — | uncertain significance |
| rs151191172 | 11:33,667,578 | G/A | — | uncertain significance |
| rs1322100986 | 11:33,667,581 | C/T | — | uncertain significance |
| rs10742301 | 11:33,668,521 | G/C | — | — |
| rs766316206 | 11:33,677,621 | C/T | — | uncertain significance |
| rs2133433051 | 11:33,677,624 | A/G | — | uncertain significance |
| rs368426217 | 11:33,680,309 | A/G | — | likely benign |
| rs957592867 | 11:33,680,382 | C/T | — | uncertain significance |
| rs759232512 | 11:33,680,396 | G/A | — | uncertain significance |
| rs190027552 | 11:33,680,408 | G/A | — | uncertain significance |
| rs368033259 | 11:33,680,412 | C/T | — | uncertain significance |
| rs750461785 | 11:33,680,417 | T/G | — | uncertain significance |
| rs369805716 | 11:33,682,557 | T/A | — | uncertain significance |
| rs537413252 | 11:33,689,459 | G/A | — | uncertain significance |
Showing 100 of 110 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.