KIAA1755
KIAA1755
Summary
Predicted to enable guanyl-nucleotide exchange factor activity. Predicted to be involved in axon guidance. Predicted to be active in cytoplasm and plasma membrane. Predicted to be extrinsic component of membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants89 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2515667390 | 20:36,841,505 | C/T | — | uncertain significance |
| rs144628188 | 20:36,841,599 | G/A | — | uncertain significance |
| rs776489100 | 20:36,841,623 | A/C | — | likely benign |
| rs2123040021 | 20:36,841,671 | G/C | — | uncertain significance |
| rs1191064440 | 20:36,841,784 | C/A | — | uncertain significance |
| rs1262421857 | 20:36,841,838 | C/T | — | uncertain significance |
| rs61748970 | 20:36,841,839 | G/A | — | benign |
| rs375138370 | 20:36,841,848 | G/A | — | uncertain significance |
| rs3746471 | 20:36,841,914 | G/A | missense variant | — |
| rs193920749 | 20:36,841,958 | C/A | — | uncertain significance |
| rs772261810 | 20:36,842,004 | C/T | — | likely benign |
| rs747051689 | 20:36,842,057 | C/T | — | uncertain significance |
| rs1410017136 | 20:36,842,134 | G/T | — | uncertain significance |
| rs6127471 | 20:36,844,038 | C/T | intron variant | — |
| rs780473853 | 20:36,845,690 | C/T | — | uncertain significance |
| rs199971628 | 20:36,845,702 | G/C | — | uncertain significance |
| rs367812234 | 20:36,845,707 | C/A | — | uncertain significance |
| rs202007256 | 20:36,845,708 | G/A | — | uncertain significance |
| rs750650900 | 20:36,845,719 | A/G | — | uncertain significance |
| rs760553122 | 20:36,845,794 | C/A | — | uncertain significance |
| rs768676447 | 20:36,845,795 | G/A | — | uncertain significance |
| rs756831857 | 20:36,845,860 | C/T | — | uncertain significance |
| rs145212886 | 20:36,845,863 | C/T | — | uncertain significance |
| rs761836863 | 20:36,845,869 | T/C | — | uncertain significance |
| rs539042122 | 20:36,846,648 | C/T | — | uncertain significance |
| rs1209514503 | 20:36,848,067 | C/T | — | likely benign |
| rs369269098 | 20:36,848,070 | G/C | — | uncertain significance |
| rs761574275 | 20:36,848,095 | G/A | — | likely benign |
| rs749835474 | 20:36,848,143 | C/A | — | uncertain significance |
| rs201309851 | 20:36,850,909 | C/T | — | uncertain significance |
| rs201601539 | 20:36,850,920 | C/T | — | uncertain significance |
| rs190340907 | 20:36,850,938 | C/T | — | uncertain significance |
| rs770635860 | 20:36,850,947 | C/G | — | uncertain significance |
| rs35524973 | 20:36,850,988 | T/C | — | uncertain significance |
| rs988541717 | 20:36,851,950 | C/A | — | uncertain significance |
| rs748304963 | 20:36,851,968 | T/C | — | uncertain significance |
| rs769748095 | 20:36,851,969 | C/G | — | uncertain significance |
| rs139388351 | 20:36,851,978 | C/T | — | likely benign |
| rs199854901 | 20:36,854,084 | A/T | — | uncertain significance |
| rs201191475 | 20:36,854,087 | C/T | — | uncertain significance |
| rs771607443 | 20:36,855,603 | C/T | — | uncertain significance |
| rs370976438 | 20:36,856,572 | C/T | — | uncertain significance |
| rs2515713212 | 20:36,856,634 | T/A | — | uncertain significance |
| rs752243158 | 20:36,859,613 | G/T | — | uncertain significance |
| rs199854032 | 20:36,859,722 | G/A | — | uncertain significance |
| rs887982542 | 20:36,867,968 | C/T | — | uncertain significance |
| rs2076017811 | 20:36,868,017 | T/C | — | uncertain significance |
| rs149656873 | 20:36,868,020 | G/A | — | uncertain significance |
| rs561609091 | 20:36,869,112 | G/A | — | uncertain significance |
| rs2515760087 | 20:36,869,144 | G/A | — | likely benign |
| rs143825509 | 20:36,869,173 | T/C | — | likely benign |
| rs1382066604 | 20:36,869,190 | C/A | — | uncertain significance |
| rs543949449 | 20:36,869,200 | C/G | — | likely benign |
| rs756684685 | 20:36,869,205 | G/A | — | uncertain significance |
| rs150187673 | 20:36,869,263 | G/A | — | uncertain significance |
| rs763161845 | 20:36,869,307 | T/G | — | uncertain significance |
| rs371537592 | 20:36,869,353 | C/G | — | uncertain significance |
| rs61745896 | 20:36,869,385 | C/G | — | benign |
| rs774534343 | 20:36,869,395 | C/T | — | uncertain significance |
| rs1001551954 | 20:36,869,421 | C/A | — | uncertain significance |
| rs765698430 | 20:36,869,430 | G/A | — | likely benign |
| rs754476109 | 20:36,869,448 | G/A | — | uncertain significance |
| rs749280186 | 20:36,869,469 | T/C | — | uncertain significance |
| rs148682562 | 20:36,869,590 | G/A | — | uncertain significance |
| rs147347811 | 20:36,869,720 | G/C | — | likely benign |
| rs758447717 | 20:36,869,743 | C/T | — | uncertain significance |
| rs780015364 | 20:36,869,744 | C/A | — | uncertain significance |
| rs373667620 | 20:36,869,794 | C/T | — | uncertain significance |
| rs968975318 | 20:36,869,851 | G/A | — | uncertain significance |
| rs751476708 | 20:36,869,858 | G/T | — | uncertain significance |
| rs2515768233 | 20:36,870,072 | T/G | — | uncertain significance |
| rs377047400 | 20:36,870,078 | G/A | — | uncertain significance |
| rs760563805 | 20:36,870,097 | T/A | — | uncertain significance |
| rs776817650 | 20:36,870,105 | A/G | — | uncertain significance |
| rs755585692 | 20:36,870,126 | A/G | — | uncertain significance |
| rs1418472652 | 20:36,870,204 | T/C | — | uncertain significance |
| rs1482000169 | 20:36,870,225 | C/A | — | uncertain significance |
| rs145701234 | 20:36,870,231 | C/T | — | uncertain significance |
| rs570239072 | 20:36,870,238 | A/T | — | uncertain significance |
| rs747989222 | 20:36,870,298 | C/A | — | uncertain significance |
| rs1318809447 | 20:36,870,327 | G/A | — | uncertain significance |
| rs376413430 | 20:36,874,362 | C/T | — | uncertain significance |
| rs775765046 | 20:36,874,363 | G/A | — | uncertain significance |
| rs777858196 | 20:36,874,410 | T/C | — | likely benign |
| rs2515784343 | 20:36,874,417 | C/T | — | uncertain significance |
| rs1482028449 | 20:36,874,443 | C/T | — | uncertain significance |
| rs762264980 | 20:36,874,462 | T/C | — | uncertain significance |
| rs1327173786 | 20:36,874,474 | G/T | — | uncertain significance |
| rs2078602 | 20:36,887,895 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.