SLIT3
slit guidance ligand 3
Summary
The protein encoded by this gene is secreted, likely interacting with roundabout homolog receptors to effect cell migration. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]
Known Variants175 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs756128556 | 5:168,093,470 | C/T | — | uncertain significance |
| rs779367410 | 5:168,093,473 | G/A | — | uncertain significance |
| rs111948103 | 5:168,093,479 | C/T | — | uncertain significance |
| rs143047334 | 5:168,093,525 | C/T | — | likely benign |
| rs762248470 | 5:168,093,550 | C/T | — | uncertain significance |
| rs140403495 | 5:168,093,559 | C/T | — | uncertain significance |
| rs1761053731 | 5:168,093,576 | C/A | — | uncertain significance |
| rs184693277 | 5:168,093,595 | C/T | — | likely benign |
| rs138032051 | 5:168,093,652 | C/T | — | likely benign |
| rs142603158 | 5:168,093,653 | G/A | — | uncertain significance |
| rs146090354 | 5:168,093,670 | A/C | — | uncertain significance |
| rs755657006 | 5:168,093,688 | G/A | — | uncertain significance |
| rs180813266 | 5:168,096,803 | C/T | — | uncertain significance |
| rs754778570 | 5:168,096,815 | C/T | — | uncertain significance |
| rs917513532 | 5:168,096,835 | G/A | — | uncertain significance |
| rs775669982 | 5:168,096,877 | T/C | — | uncertain significance |
| rs766182517 | 5:168,096,928 | C/T | — | uncertain significance |
| rs1462312638 | 5:168,096,959 | A/G | — | uncertain significance |
| rs2113166572 | 5:168,096,970 | G/T | — | uncertain significance |
| rs372559587 | 5:168,098,233 | T/C | — | uncertain significance |
| rs2277933 | 5:168,098,235 | A/G | — | benign |
| rs150953871 | 5:168,098,250 | G/A | — | likely benign |
| rs149659886 | 5:168,098,277 | C/T | — | likely benign |
| rs372876846 | 5:168,098,286 | C/A | — | uncertain significance |
| rs148891683 | 5:168,098,331 | C/T | — | benign |
| rs1475946909 | 5:168,098,359 | T/G | — | uncertain significance |
| rs2546428148 | 5:168,098,370 | G/T | — | likely benign |
| rs1761236927 | 5:168,098,383 | T/A | — | uncertain significance |
| rs757648989 | 5:168,098,385 | C/T | — | likely benign |
| rs754469833 | 5:168,098,407 | T/A | — | uncertain significance |
| rs1582511364 | 5:168,098,412 | G/A | — | likely benign |
| rs35568421 | 5:168,098,427 | G/A | — | benign |
| rs292486 | 5:168,098,463 | A/G | — | benign |
| rs199921593 | 5:168,098,471 | C/T | — | uncertain significance |
| rs1223858431 | 5:168,100,240 | G/A | — | likely benign |
| rs201023586 | 5:168,100,281 | G/T | — | uncertain significance |
| rs1427892240 | 5:168,111,055 | T/C | — | uncertain significance |
| rs766120712 | 5:168,111,091 | T/G | — | uncertain significance |
| rs1035584913 | 5:168,111,101 | C/T | — | uncertain significance |
| rs72839508 | 5:168,112,707 | G/A | — | likely benign |
| rs144799628 | 5:168,112,742 | C/G | — | likely benign |
| rs774066209 | 5:168,112,769 | C/T | — | uncertain significance |
| rs1424624849 | 5:168,112,793 | G/A | — | uncertain significance |
| rs774614436 | 5:168,112,882 | G/T | — | uncertain significance |
| rs754398981 | 5:168,112,914 | G/T | — | uncertain significance |
| rs747954140 | 5:168,114,002 | G/A | — | likely benign |
| rs148887706 | 5:168,114,030 | C/T | — | uncertain significance |
| rs754304771 | 5:168,114,065 | C/T | — | uncertain significance |
| rs762085322 | 5:168,114,068 | T/C | — | uncertain significance |
| rs1291488100 | 5:168,114,094 | C/T | — | likely benign |
| rs777961394 | 5:168,119,665 | C/G | — | uncertain significance |
| rs201687321 | 5:168,119,692 | G/A | — | likely benign |
| rs577752594 | 5:168,119,700 | G/A | — | likely benign |
| rs144483314 | 5:168,123,324 | C/T | — | uncertain significance |
| rs201684175 | 5:168,123,326 | T/A | — | uncertain significance |
| rs61746224 | 5:168,123,346 | G/A | — | likely benign |
| rs776317879 | 5:168,123,375 | C/T | — | uncertain significance |
| rs2546450420 | 5:168,123,384 | C/T | — | uncertain significance |
| rs1454938390 | 5:168,123,388 | T/C | — | likely benign |
| rs769550253 | 5:168,123,404 | C/T | — | uncertain significance |
| rs140275746 | 5:168,127,655 | G/A | — | likely benign |
| rs368820028 | 5:168,127,669 | C/T | — | uncertain significance |
| rs764682671 | 5:168,135,020 | A/G | — | likely benign |
| rs368724395 | 5:168,137,891 | G/A | — | benign |
| rs752599328 | 5:168,137,965 | C/T | — | uncertain significance |
| rs758437974 | 5:168,137,976 | G/A | — | likely benign |
| rs370937958 | 5:168,137,998 | G/A | — | uncertain significance |
| rs141936653 | 5:168,138,060 | C/T | — | likely benign |
| rs116584490 | 5:168,139,279 | G/A | — | benign |
| rs35807688 | 5:168,139,310 | C/T | — | benign |
| rs2546464613 | 5:168,139,312 | T/C | — | uncertain significance |
| rs77214174 | 5:168,147,294 | T/C | — | uncertain significance |
| rs2546475789 | 5:168,149,297 | A/G | — | uncertain significance |
| rs1411118757 | 5:168,149,955 | C/T | — | uncertain significance |
| rs149709542 | 5:168,149,956 | A/G | — | uncertain significance |
| rs144594798 | 5:168,151,427 | G/A | — | uncertain significance |
| rs138524475 | 5:168,151,443 | C/T | — | uncertain significance |
| rs142385399 | 5:168,166,731 | G/C | — | — |
| rs372330697 | 5:168,175,344 | C/T | — | uncertain significance |
| rs202026700 | 5:168,175,371 | C/T | — | uncertain significance |
| rs147915250 | 5:168,175,408 | C/T | — | likely benign |
| rs1008352683 | 5:168,176,485 | G/A | — | uncertain significance |
| rs138307962 | 5:168,176,569 | C/T | — | uncertain significance |
| rs996605370 | 5:168,176,572 | C/T | — | uncertain significance |
| rs371722412 | 5:168,176,575 | T/A | — | uncertain significance |
| rs2546504174 | 5:168,176,624 | G/T | — | uncertain significance |
| rs564408745 | 5:168,179,981 | G/A | — | uncertain significance |
| rs765735352 | 5:168,179,999 | G/T | — | uncertain significance |
| rs34260167 | 5:168,180,047 | T/C | — | benign |
| rs202128265 | 5:168,180,054 | C/T | — | uncertain significance |
| rs10036727 | 5:168,180,081 | T/C | — | benign |
| rs1279530013 | 5:168,180,879 | G/T | — | uncertain significance |
| rs577365804 | 5:168,180,894 | G/A | — | likely benign |
| rs145457028 | 5:168,180,900 | C/T | — | benign |
| rs763629847 | 5:168,180,913 | G/A | — | likely benign |
| rs758069520 | 5:168,180,951 | C/T | — | uncertain significance |
| rs751501759 | 5:168,180,966 | C/T | — | uncertain significance |
| rs755024709 | 5:168,187,873 | C/T | — | uncertain significance |
| rs767560268 | 5:168,187,874 | G/A | — | uncertain significance |
| rs1292544343 | 5:168,187,883 | G/C | — | uncertain significance |
Showing 100 of 175 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.