ROBO4
roundabout guidance receptor 4
Summary
Predicted to enable cell-cell adhesion mediator activity. Involved in establishment of endothelial barrier. Located in extracellular exosome. Implicated in aortic valve disease 3. Biomarker of pre-eclampsia and thyroid gland carcinoma. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants162 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs376405868 | 11:124,754,797 | T/C | — | uncertain significance |
| rs145918924 | 11:124,754,934 | T/C | — | benign |
| rs548878110 | 11:124,754,943 | C/T | — | uncertain significance |
| rs1946688642 | 11:124,754,957 | C/T | — | uncertain significance |
| rs571041984 | 11:124,754,987 | T/G | — | uncertain significance |
| rs368968468 | 11:124,755,026 | C/T | — | uncertain significance |
| rs774960443 | 11:124,755,027 | G/A | — | uncertain significance |
| rs148605539 | 11:124,755,031 | G/A | — | benign |
| rs2497353826 | 11:124,755,033 | T/G | — | uncertain significance |
| rs142085681 | 11:124,755,072 | A/G | — | uncertain significance |
| rs2497354377 | 11:124,755,104 | A/G | — | uncertain significance |
| rs201729497 | 11:124,755,116 | T/A | — | uncertain significance |
| rs774923165 | 11:124,755,125 | G/A | — | uncertain significance |
| rs374357392 | 11:124,756,382 | C/A | — | uncertain significance |
| rs2497358798 | 11:124,756,395 | C/T | — | uncertain significance |
| rs529793135 | 11:124,756,396 | C/T | — | uncertain significance |
| rs200670182 | 11:124,756,397 | G/C | — | uncertain significance |
| rs7104934 | 11:124,756,406 | G/A | — | benign |
| rs377333725 | 11:124,756,432 | G/A | — | uncertain significance |
| rs767574908 | 11:124,756,465 | C/T | — | uncertain significance |
| rs1202507925 | 11:124,756,518 | G/A | — | uncertain significance |
| rs766605330 | 11:124,756,593 | C/T | — | uncertain significance |
| rs149560585 | 11:124,756,683 | G/C | — | uncertain significance |
| rs2135366023 | 11:124,756,919 | C/A | — | likely pathogenic |
| rs144947842 | 11:124,756,981 | C/T | — | likely benign |
| rs138481093 | 11:124,756,982 | G/A | — | likely benign |
| rs141824908 | 11:124,757,025 | G/T | — | uncertain significance |
| rs146276743 | 11:124,757,029 | G/A | — | benign |
| rs1035554890 | 11:124,757,075 | G/T | — | uncertain significance |
| rs1044113961 | 11:124,757,270 | G/A | — | uncertain significance |
| rs150534997 | 11:124,757,279 | G/A | — | uncertain significance |
| rs139537489 | 11:124,757,281 | G/A | — | uncertain significance |
| rs74979341 | 11:124,757,299 | G/A | — | benign |
| rs990952264 | 11:124,757,309 | G/A | — | uncertain significance |
| rs147340062 | 11:124,757,317 | C/T | — | likely benign |
| rs139471672 | 11:124,757,328 | C/A | — | uncertain significance |
| rs377742325 | 11:124,757,352 | C/A | — | likely benign |
| rs749631326 | 11:124,757,353 | G/A | — | uncertain significance |
| rs149262190 | 11:124,757,360 | G/T | — | uncertain significance |
| rs761647720 | 11:124,757,374 | A/G | — | uncertain significance |
| rs764038221 | 11:124,757,628 | C/A | — | likely pathogenic |
| rs761883031 | 11:124,757,646 | T/A | — | uncertain significance |
| rs4408324 | 11:124,757,679 | C/T | — | benign |
| rs199554824 | 11:124,757,680 | G/A | — | likely benign |
| rs140966335 | 11:124,757,687 | C/T | — | likely benign |
| rs145067866 | 11:124,757,700 | C/T | — | conflicting classifications of pathogenicity |
| rs749066541 | 11:124,757,703 | C/T | — | uncertain significance |
| rs772059095 | 11:124,757,721 | T/C | — | uncertain significance |
| rs6590109 | 11:124,759,048 | G/A | downstream gene variant | — |
| rs369176966 | 11:124,761,206 | T/C | — | uncertain significance |
| rs2497376190 | 11:124,761,210 | C/A | — | uncertain significance |
| rs958298127 | 11:124,761,220 | C/A | — | uncertain significance |
| rs140544911 | 11:124,761,242 | C/T | — | uncertain significance |
| rs145535350 | 11:124,761,243 | G/A | — | conflicting classifications of pathogenicity |
| rs1463214202 | 11:124,761,248 | G/T | — | uncertain significance |
| rs372455722 | 11:124,761,257 | C/T | — | uncertain significance |
| rs138111911 | 11:124,761,279 | C/G | — | likely pathogenic |
| rs751371459 | 11:124,761,318 | G/C | — | uncertain significance |
| rs149507368 | 11:124,761,326 | C/T | — | likely benign |
| rs749338809 | 11:124,761,327 | G/A | — | uncertain significance |
| rs1041512303 | 11:124,761,345 | G/C | — | uncertain significance |
| rs772195431 | 11:124,761,354 | G/T | — | uncertain significance |
| rs143995311 | 11:124,761,368 | C/T | — | benign |
| rs946298494 | 11:124,761,372 | A/G | — | uncertain significance |
| rs111626453 | 11:124,761,385 | G/T | — | likely benign |
| rs751354937 | 11:124,761,398 | T/A | — | uncertain significance |
| rs201492213 | 11:124,761,441 | G/A | — | conflicting classifications of pathogenicity |
| rs59946255 | 11:124,761,456 | G/A | — | benign |
| rs145076728 | 11:124,761,568 | G/A | — | uncertain significance |
| rs370414211 | 11:124,761,570 | C/G | — | uncertain significance |
| rs199901174 | 11:124,761,571 | G/A | — | uncertain significance |
| rs760325971 | 11:124,761,583 | G/A | — | uncertain significance |
| rs201366848 | 11:124,761,596 | C/T | — | benign |
| rs536213620 | 11:124,761,606 | C/T | — | uncertain significance |
| rs145116773 | 11:124,761,607 | G/A | — | benign |
| rs567828905 | 11:124,761,643 | A/G | — | uncertain significance |
| rs192892799 | 11:124,761,657 | C/T | — | uncertain significance |
| rs777955565 | 11:124,761,676 | A/G | — | uncertain significance |
| rs1565325937 | 11:124,763,602 | T/A | — | uncertain significance |
| rs765547083 | 11:124,763,606 | C/T | — | likely benign |
| rs1211608718 | 11:124,763,771 | C/A | — | uncertain significance |
| rs374471211 | 11:124,763,789 | G/A | — | uncertain significance |
| rs564107859 | 11:124,763,792 | G/C | — | benign |
| rs772019553 | 11:124,763,801 | C/T | — | uncertain significance |
| rs74458892 | 11:124,763,802 | G/A | — | benign |
| rs1339065641 | 11:124,763,836 | C/T | — | uncertain significance |
| rs760068022 | 11:124,763,837 | C/T | — | uncertain significance |
| rs141436705 | 11:124,763,860 | C/T | — | uncertain significance |
| rs2497388726 | 11:124,763,897 | G/C | — | uncertain significance |
| rs373760832 | 11:124,763,902 | T/A | — | uncertain significance |
| rs1373878480 | 11:124,764,127 | C/T | — | uncertain significance |
| rs868068837 | 11:124,764,135 | C/A | — | uncertain significance |
| rs1044860455 | 11:124,764,153 | G/A | — | uncertain significance |
| rs751373555 | 11:124,764,163 | C/T | — | uncertain significance |
| rs11820142 | 11:124,764,176 | T/C | — | benign |
| rs1565326476 | 11:124,764,182 | A/T | — | likely pathogenic |
| rs372037630 | 11:124,764,190 | C/T | — | uncertain significance |
| rs769202799 | 11:124,764,196 | C/T | — | uncertain significance |
| rs1315701245 | 11:124,764,255 | A/G | — | uncertain significance |
| rs199617085 | 11:124,764,265 | C/T | — | benign |
Showing 100 of 162 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.