MEGF11
multiple EGF like domains 11
Summary
Predicted to be involved in homotypic cell-cell adhesion and retina layer formation. Predicted to be located in basolateral plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants81 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs761644531 | 15:66,190,277 | A/G | — | uncertain significance |
| rs370404367 | 15:66,190,294 | G/A | — | uncertain significance |
| rs747064732 | 15:66,190,361 | G/A | — | uncertain significance |
| rs267604294 | 15:66,190,367 | C/T | — | uncertain significance |
| rs1455390732 | 15:66,190,391 | A/C | — | uncertain significance |
| rs759920937 | 15:66,191,264 | T/C | — | uncertain significance |
| rs766132021 | 15:66,198,470 | C/T | — | uncertain significance |
| rs1207318315 | 15:66,206,125 | A/G | — | uncertain significance |
| rs757871149 | 15:66,206,129 | G/A | — | uncertain significance |
| rs150945752 | 15:66,206,161 | C/T | missense variant | Uncertain significance |
| rs747004559 | 15:66,206,165 | G/A | — | uncertain significance |
| rs768551955 | 15:66,206,167 | C/T | — | uncertain significance |
| rs150125637 | 15:66,206,228 | T/G | — | uncertain significance |
| rs2549081884 | 15:66,206,254 | G/A | — | uncertain significance |
| rs759073662 | 15:66,206,278 | G/A | — | uncertain significance |
| rs1162233276 | 15:66,206,294 | C/T | — | uncertain significance |
| rs903451611 | 15:66,206,308 | G/A | — | uncertain significance |
| rs746173752 | 15:66,208,579 | G/A | — | uncertain significance |
| rs373932693 | 15:66,208,591 | T/C | — | uncertain significance |
| rs373679622 | 15:66,209,234 | G/C | — | uncertain significance |
| rs560793386 | 15:66,210,309 | G/A | — | uncertain significance |
| rs762469413 | 15:66,210,373 | C/T | — | uncertain significance |
| rs761151605 | 15:66,210,376 | T/C | — | uncertain significance |
| rs1183879536 | 15:66,210,381 | G/A | — | uncertain significance |
| rs764487794 | 15:66,214,715 | C/G | — | uncertain significance |
| rs143395466 | 15:66,214,724 | C/T | — | uncertain significance |
| rs1244790767 | 15:66,214,753 | T/C | — | uncertain significance |
| rs747837275 | 15:66,214,778 | C/T | — | uncertain significance |
| rs777394739 | 15:66,214,784 | C/T | — | likely benign |
| rs1161054584 | 15:66,215,229 | C/A | — | uncertain significance |
| rs201935452 | 15:66,215,241 | C/G | — | uncertain significance |
| rs765973342 | 15:66,215,281 | G/A | — | likely benign |
| rs1203703970 | 15:66,215,293 | T/C | — | uncertain significance |
| rs144721492 | 15:66,215,301 | C/T | — | likely benign |
| rs141706671 | 15:66,215,302 | G/A | — | uncertain significance |
| rs554311397 | 15:66,222,059 | G/A | — | uncertain significance |
| rs2549129084 | 15:66,222,074 | C/T | — | uncertain significance |
| rs2549129614 | 15:66,222,163 | G/C | — | uncertain significance |
| rs778987546 | 15:66,223,184 | T/C | — | uncertain significance |
| rs761111884 | 15:66,223,245 | A/G | — | uncertain significance |
| rs141697214 | 15:66,223,266 | C/T | — | likely benign |
| rs748726700 | 15:66,249,961 | T/C | — | uncertain significance |
| rs369322234 | 15:66,257,262 | C/T | — | uncertain significance |
| rs751149953 | 15:66,257,338 | C/A | — | uncertain significance |
| rs145416652 | 15:66,257,436 | C/T | — | uncertain significance |
| rs72625765 | 15:66,260,432 | G/A | — | — |
| rs139555084 | 15:66,262,934 | C/T | — | uncertain significance |
| rs765597002 | 15:66,262,993 | G/A | — | uncertain significance |
| rs755103840 | 15:66,263,011 | T/C | — | uncertain significance |
| rs201325700 | 15:66,273,117 | G/A | — | uncertain significance |
| rs780630175 | 15:66,273,142 | C/T | — | uncertain significance |
| rs1178923552 | 15:66,273,177 | C/A | — | uncertain significance |
| rs764436181 | 15:66,273,183 | C/G | — | uncertain significance |
| rs145333107 | 15:66,273,187 | G/T | — | uncertain significance |
| rs764755239 | 15:66,274,584 | C/G | — | uncertain significance |
| rs2081673477 | 15:66,274,617 | C/T | — | uncertain significance |
| rs1404095661 | 15:66,274,671 | C/T | — | uncertain significance |
| rs757787591 | 15:66,274,704 | C/T | — | uncertain significance |
| rs760275330 | 15:66,274,718 | C/T | — | uncertain significance |
| rs1372488435 | 15:66,274,719 | G/A | — | uncertain significance |
| rs2081684241 | 15:66,274,755 | G/A | — | uncertain significance |
| rs749371493 | 15:66,274,784 | C/A | — | uncertain significance |
| rs774237193 | 15:66,274,788 | G/C | — | uncertain significance |
| rs2081687361 | 15:66,274,815 | C/G | — | uncertain significance |
| rs760395422 | 15:66,274,819 | G/C | — | uncertain significance |
| rs369433774 | 15:66,386,741 | G/T | — | uncertain significance |
| rs753304245 | 15:66,386,797 | C/T | — | uncertain significance |
| rs201352763 | 15:66,386,802 | C/T | — | uncertain significance |
| rs1298570187 | 15:66,386,806 | C/T | — | uncertain significance |
| rs145640631 | 15:66,386,823 | G/A | — | uncertain significance |
| rs1371637923 | 15:66,411,465 | T/C | — | uncertain significance |
| rs779786134 | 15:66,411,478 | G/A | — | uncertain significance |
| rs1479607738 | 15:66,411,489 | C/T | — | uncertain significance |
| rs750694093 | 15:66,411,507 | G/A | — | uncertain significance |
| rs2544030121 | 15:66,416,243 | C/A | — | uncertain significance |
| rs770643356 | 15:66,416,277 | A/G | — | uncertain significance |
| rs1274386732 | 15:66,420,650 | C/A | — | uncertain significance |
| rs750210212 | 15:66,420,663 | C/T | — | uncertain significance |
| rs139006288 | 15:66,420,724 | C/T | — | likely benign |
| rs1477798 | 15:66,452,246 | T/C | intron variant | — |
| rs118122709 | 15:66,501,376 | G/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.