EGFLAM
EGF like, fibronectin type III and laminin G domains
Summary
Predicted to enable calcium ion binding activity and glycosaminoglycan binding activity. Predicted to act upstream of or within extracellular matrix organization and positive regulation of cell-substrate adhesion. Part of cell surface. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants79 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs371610360 | 5:38,258,870 | G/A | — | uncertain significance |
| rs779458784 | 5:38,337,724 | G/A | — | uncertain significance |
| rs141979824 | 5:38,338,852 | G/A | — | uncertain significance |
| rs764687373 | 5:38,338,866 | C/T | — | uncertain significance |
| rs141310046 | 5:38,338,882 | C/T | — | uncertain significance |
| rs543782279 | 5:38,350,604 | A/G | — | uncertain significance |
| rs761096359 | 5:38,350,642 | C/T | — | uncertain significance |
| rs780233990 | 5:38,350,693 | C/A | — | uncertain significance |
| rs1385634607 | 5:38,350,697 | G/A | — | likely benign |
| rs148290116 | 5:38,350,704 | C/G | — | likely benign |
| rs773572869 | 5:38,352,303 | T/G | — | uncertain significance |
| rs771395994 | 5:38,352,312 | C/A | — | uncertain significance |
| rs377637249 | 5:38,352,315 | G/C | — | uncertain significance |
| rs180977046 | 5:38,352,349 | C/T | — | uncertain significance |
| rs1398082504 | 5:38,352,361 | T/C | — | uncertain significance |
| rs1217883680 | 5:38,352,388 | G/C | — | uncertain significance |
| rs1465567 | 5:38,370,537 | C/T | — | benign |
| rs2921222 | 5:38,375,185 | G/A | intron variant | — |
| rs10472302 | 5:38,388,894 | G/A | intron variant | — |
| rs1443689893 | 5:38,394,593 | G/C | — | — |
| rs762335917 | 5:38,406,260 | C/T | — | uncertain significance |
| rs758048079 | 5:38,406,297 | A/G | — | uncertain significance |
| rs2530768634 | 5:38,406,320 | G/T | — | uncertain significance |
| rs371899172 | 5:38,407,005 | C/A | — | uncertain significance |
| rs1379131478 | 5:38,407,173 | T/C | — | uncertain significance |
| rs561735667 | 5:38,407,201 | C/T | — | uncertain significance |
| rs141957279 | 5:38,407,221 | G/A | — | uncertain significance |
| rs201837940 | 5:38,407,230 | G/A | — | uncertain significance |
| rs555414321 | 5:38,407,979 | A/G | — | uncertain significance |
| rs1391961685 | 5:38,409,170 | T/C | — | uncertain significance |
| rs150754556 | 5:38,412,616 | G/A | — | uncertain significance |
| rs202118362 | 5:38,412,637 | G/A | — | likely benign |
| rs1378080933 | 5:38,412,647 | C/A | — | uncertain significance |
| rs1561077403 | 5:38,412,695 | G/T | — | uncertain significance |
| rs201151464 | 5:38,412,731 | C/T | — | uncertain significance |
| rs755120286 | 5:38,418,225 | G/A | — | uncertain significance |
| rs200385131 | 5:38,418,236 | G/T | — | uncertain significance |
| rs200770771 | 5:38,418,321 | T/C | — | uncertain significance |
| rs373444710 | 5:38,425,140 | G/A | — | uncertain significance |
| rs766867269 | 5:38,427,170 | T/C | — | uncertain significance |
| rs374749456 | 5:38,427,177 | T/C | — | uncertain significance |
| rs199504103 | 5:38,427,281 | T/A | — | uncertain significance |
| rs2530813339 | 5:38,427,290 | A/C | — | uncertain significance |
| rs545316137 | 5:38,427,298 | G/C | — | uncertain significance |
| rs140090894 | 5:38,427,316 | G/T | — | uncertain significance |
| rs2530813590 | 5:38,427,324 | T/C | — | uncertain significance |
| rs201011365 | 5:38,435,266 | A/G | — | uncertain significance |
| rs202234341 | 5:38,435,294 | A/G | — | likely benign |
| rs202176859 | 5:38,435,296 | T/C | — | uncertain significance |
| rs115665295 | 5:38,435,318 | C/T | — | uncertain significance |
| rs369952716 | 5:38,438,380 | A/G | — | uncertain significance |
| rs376633900 | 5:38,438,408 | A/C | — | uncertain significance |
| rs368992352 | 5:38,438,428 | G/A | — | uncertain significance |
| rs567359987 | 5:38,438,429 | T/C | — | uncertain significance |
| rs1742423561 | 5:38,438,464 | G/A | — | uncertain significance |
| rs200790571 | 5:38,438,491 | C/T | — | uncertain significance |
| rs778276251 | 5:38,445,792 | T/C | — | uncertain significance |
| rs554091075 | 5:38,448,403 | C/T | — | uncertain significance |
| rs1008245666 | 5:38,448,427 | C/T | — | uncertain significance |
| rs780497462 | 5:38,448,442 | G/A | — | uncertain significance |
| rs1742794145 | 5:38,448,465 | C/G | — | uncertain significance |
| rs767522576 | 5:38,451,449 | G/A | — | uncertain significance |
| rs147320207 | 5:38,451,504 | G/A | — | uncertain significance |
| rs1349728910 | 5:38,451,536 | T/C | — | uncertain significance |
| rs138983512 | 5:38,451,538 | C/T | — | uncertain significance |
| rs1742911042 | 5:38,451,544 | G/A | — | uncertain significance |
| rs1206794025 | 5:38,451,550 | C/A | — | uncertain significance |
| rs7715172 | 5:38,452,894 | C/T | — | — |
| rs35230295 | 5:38,458,464 | C/T | — | benign |
| rs202035735 | 5:38,458,472 | G/A | — | uncertain significance |
| rs371848483 | 5:38,458,491 | C/T | — | likely benign |
| rs750381529 | 5:38,463,043 | C/A | — | uncertain significance |
| rs780208688 | 5:38,463,045 | A/G | — | uncertain significance |
| rs772568999 | 5:38,463,081 | G/A | — | uncertain significance |
| rs953112738 | 5:38,463,086 | C/T | — | uncertain significance |
| rs761267268 | 5:38,463,096 | A/G | — | uncertain significance |
| rs140904490 | 5:38,463,954 | C/G | — | uncertain significance |
| rs371582383 | 5:38,463,987 | G/T | — | uncertain significance |
| rs1233239972 | 5:38,464,009 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.