ABI3BP
ABI family member 3 binding protein
Summary
Predicted to enable actin filament binding activity. Predicted to be involved in several processes, including extracellular matrix organization; positive regulation of cell-substrate adhesion; and regulation of postsynapse organization. Located in collagen-containing extracellular matrix and extracellular space. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants73 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs575309030 | 3:100,470,401 | T/A | — | uncertain significance |
| rs781305468 | 3:100,470,509 | T/C | — | uncertain significance |
| rs1378697834 | 3:100,471,673 | T/G | — | uncertain significance |
| rs2472524421 | 3:100,471,751 | C/T | — | uncertain significance |
| rs2472639409 | 3:100,472,684 | T/C | — | uncertain significance |
| rs9823506 | 3:100,476,713 | C/T | intron variant | — |
| rs971230 | 3:100,478,315 | C/G | regulatory region variant | — |
| rs1022907412 | 3:100,489,704 | C/A | — | uncertain significance |
| rs370738785 | 3:100,489,737 | C/T | — | uncertain significance |
| rs2474546036 | 3:100,493,453 | G/T | — | uncertain significance |
| rs1190390654 | 3:100,493,460 | G/A | — | uncertain significance |
| rs1212419561 | 3:100,494,139 | C/A | — | uncertain significance |
| rs775925923 | 3:100,497,211 | C/T | — | uncertain significance |
| rs376392494 | 3:100,499,027 | C/G | — | uncertain significance |
| rs2475083860 | 3:100,499,050 | A/T | — | uncertain significance |
| rs7613610 | 3:100,499,321 | C/T | — | — |
| rs9850273 | 3:100,499,365 | G/A | intron variant | — |
| rs745850997 | 3:100,508,345 | T/C | — | uncertain significance |
| rs769685696 | 3:100,508,351 | C/A | — | uncertain significance |
| rs374566927 | 3:100,508,360 | G/A | — | uncertain significance |
| rs2097232511 | 3:100,511,582 | A/G | — | uncertain significance |
| rs1373428474 | 3:100,511,588 | T/C | — | uncertain significance |
| rs2476799434 | 3:100,513,839 | C/T | — | uncertain significance |
| rs758400863 | 3:100,515,273 | T/C | — | uncertain significance |
| rs367999543 | 3:100,515,301 | C/G | — | uncertain significance |
| rs1210997866 | 3:100,527,007 | G/T | — | uncertain significance |
| rs202241381 | 3:100,527,031 | C/T | — | likely benign |
| rs768551201 | 3:100,527,061 | C/T | — | uncertain significance |
| rs372669157 | 3:100,566,448 | G/A | — | likely benign |
| rs778719617 | 3:100,566,452 | T/C | — | uncertain significance |
| rs2485850130 | 3:100,567,656 | C/T | — | uncertain significance |
| rs758085834 | 3:100,567,672 | G/A | — | uncertain significance |
| rs748429277 | 3:100,568,896 | C/T | — | likely benign |
| rs2486131604 | 3:100,569,510 | T/G | — | uncertain significance |
| rs200613525 | 3:100,569,528 | G/A | — | uncertain significance |
| rs1247948882 | 3:100,581,187 | G/A | — | uncertain significance |
| rs775517608 | 3:100,583,730 | C/T | — | uncertain significance |
| rs1331967205 | 3:100,585,735 | G/C | — | uncertain significance |
| rs376666268 | 3:100,585,752 | A/G | — | uncertain significance |
| rs1020064203 | 3:100,585,777 | G/C | — | uncertain significance |
| rs369376979 | 3:100,585,785 | A/C | — | uncertain significance |
| rs9848726 | 3:100,590,822 | A/T | intron variant | — |
| rs9833094 | 3:100,590,925 | C/A | — | — |
| rs376449327 | 3:100,593,691 | G/C | — | uncertain significance |
| rs373818981 | 3:100,593,730 | C/T | — | likely benign |
| rs1308851566 | 3:100,593,760 | C/A | — | uncertain significance |
| rs182100909 | 3:100,593,769 | T/C | — | likely benign |
| rs2099153255 | 3:100,594,373 | G/A | — | uncertain significance |
| rs754941790 | 3:100,594,404 | G/C | — | uncertain significance |
| rs747953902 | 3:100,594,408 | G/A | — | uncertain significance |
| rs373245696 | 3:100,595,386 | T/C | — | uncertain significance |
| rs191960195 | 3:100,595,400 | G/A | — | uncertain significance |
| rs2491153276 | 3:100,604,382 | C/T | — | uncertain significance |
| rs1395112313 | 3:100,604,391 | C/A | — | uncertain significance |
| rs751371978 | 3:100,604,399 | T/C | — | uncertain significance |
| rs2491159291 | 3:100,604,406 | T/C | — | uncertain significance |
| rs776801439 | 3:100,604,998 | T/C | — | uncertain significance |
| rs1335500729 | 3:100,605,044 | T/A | — | uncertain significance |
| rs1190197549 | 3:100,617,699 | C/T | — | uncertain significance |
| rs182876905 | 3:100,617,729 | C/T | — | uncertain significance |
| rs142287284 | 3:100,627,655 | T/C | downstream gene variant | — |
| rs2153640039 | 3:100,645,184 | G/C | — | uncertain significance |
| rs765606376 | 3:100,645,191 | A/G | — | uncertain significance |
| rs369448250 | 3:100,645,241 | T/C | — | uncertain significance |
| rs200989560 | 3:100,645,246 | A/T | — | uncertain significance |
| rs1306785051 | 3:100,645,275 | G/T | — | uncertain significance |
| rs9827694 | 3:100,648,298 | G/A | regulatory region variant | — |
| rs9843102 | 3:100,650,929 | G/A | intron variant | — |
| rs115920108 | 3:100,656,639 | G/A | intron variant | — |
| rs532797767 | 3:100,682,572 | C/T | — | — |
| rs1490845666 | 3:100,712,165 | G/C | — | uncertain significance |
| rs978373519 | 3:100,712,173 | C/T | — | uncertain significance |
| rs901739111 | 3:100,712,197 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.