ELFN2
extracellular leucine rich repeat and fibronectin type III domain containing 2
Summary
Predicted to enable protein phosphatase inhibitor activity. Predicted to be involved in synaptic membrane adhesion. Predicted to act upstream of or within chemical synaptic transmission; establishment of protein localization; and gene expression. Located in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs144488226 | 22:37,769,233 | C/T | — | uncertain significance |
| rs780401854 | 22:37,769,278 | G/A | — | uncertain significance |
| rs754011945 | 22:37,769,285 | C/G | — | uncertain significance |
| rs1487961281 | 22:37,769,341 | T/C | — | uncertain significance |
| rs2517709889 | 22:37,769,357 | C/T | — | uncertain significance |
| rs746833926 | 22:37,769,369 | G/A | — | uncertain significance |
| rs1287690574 | 22:37,769,395 | C/T | — | uncertain significance |
| rs758428953 | 22:37,769,435 | C/T | — | uncertain significance |
| rs745636836 | 22:37,769,452 | T/C | — | uncertain significance |
| rs781726017 | 22:37,769,630 | C/G | — | uncertain significance |
| rs199787830 | 22:37,769,699 | G/A | — | likely benign |
| rs1332195647 | 22:37,769,728 | C/T | — | uncertain significance |
| rs779305364 | 22:37,769,771 | G/C | — | uncertain significance |
| rs566547957 | 22:37,769,996 | C/T | — | uncertain significance |
| rs376827195 | 22:37,770,010 | G/A | — | uncertain significance |
| rs746549719 | 22:37,770,028 | C/G | — | uncertain significance |
| rs770420117 | 22:37,770,038 | C/T | — | uncertain significance |
| rs149473582 | 22:37,770,044 | C/T | — | uncertain significance |
| rs143903281 | 22:37,770,047 | C/T | — | uncertain significance |
| rs150864906 | 22:37,770,155 | G/A | — | uncertain significance |
| rs762922500 | 22:37,770,212 | C/T | — | uncertain significance |
| rs748776432 | 22:37,770,237 | A/T | — | uncertain significance |
| rs2517711614 | 22:37,770,296 | C/G | — | uncertain significance |
| rs141391258 | 22:37,770,356 | C/T | — | uncertain significance |
| rs768664794 | 22:37,770,359 | A/C | — | uncertain significance |
| rs202156863 | 22:37,770,469 | C/T | — | uncertain significance |
| rs572435588 | 22:37,770,494 | C/A | — | uncertain significance |
| rs763718944 | 22:37,770,599 | C/T | — | uncertain significance |
| rs182966816 | 22:37,770,661 | G/A | — | uncertain significance |
| rs149419442 | 22:37,770,699 | A/C | — | uncertain significance |
| rs759831341 | 22:37,770,703 | G/A | — | uncertain significance |
| rs775970688 | 22:37,770,788 | T/G | — | uncertain significance |
| rs6000698 | 22:37,770,790 | G/T | — | benign |
| rs757543769 | 22:37,770,797 | G/A | — | uncertain significance |
| rs373976213 | 22:37,770,838 | C/T | — | uncertain significance |
| rs572323623 | 22:37,770,919 | C/T | — | uncertain significance |
| rs965657453 | 22:37,771,109 | T/G | — | uncertain significance |
| rs2517713370 | 22:37,771,214 | C/T | — | uncertain significance |
| rs151050985 | 22:37,771,348 | T/C | — | benign |
| rs368781861 | 22:37,771,513 | C/T | — | uncertain significance |
| rs192857772 | 22:37,824,152 | G/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.