FBLN7
fibulin 7
Summary
Predicted to enable calcium ion binding activity; heparan sulfate proteoglycan binding activity; and heparin binding activity. Predicted to be involved in cell adhesion. Located in focal adhesion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs759455796 | 2:112,896,240 | C/T | — | uncertain significance |
| rs199704935 | 2:112,896,267 | T/C | — | uncertain significance |
| rs537394233 | 2:112,897,039 | C/A | — | — |
| rs4849044 | 2:112,898,933 | C/T | intron variant | — |
| rs1681624852 | 2:112,917,284 | C/T | — | uncertain significance |
| rs1326767381 | 2:112,917,338 | G/A | — | uncertain significance |
| rs758061934 | 2:112,917,398 | C/A | — | uncertain significance |
| rs746771939 | 2:112,917,406 | C/T | — | uncertain significance |
| rs113858761 | 2:112,918,469 | T/G | regulatory region variant | — |
| rs34870326 | 2:112,922,588 | G/A | — | likely benign |
| rs1573800425 | 2:112,922,683 | T/A | — | uncertain significance |
| rs10864900 | 2:112,929,485 | G/A | intron variant | — |
| rs149363704 | 2:112,933,392 | C/T | — | uncertain significance |
| rs2466823639 | 2:112,939,321 | C/G | — | uncertain significance |
| rs1342297236 | 2:112,939,326 | G/C | — | uncertain significance |
| rs1259787119 | 2:112,939,358 | G/T | — | uncertain significance |
| rs756399788 | 2:112,939,373 | C/A | — | uncertain significance |
| rs147423265 | 2:112,940,369 | C/T | — | likely benign |
| rs2466829016 | 2:112,940,422 | A/G | — | uncertain significance |
| rs369700908 | 2:112,940,424 | G/A | — | likely benign |
| rs373897520 | 2:112,940,440 | C/T | — | uncertain significance |
| rs760028458 | 2:112,940,458 | C/T | — | uncertain significance |
| rs147173660 | 2:112,940,490 | G/A | — | uncertain significance |
| rs560016257 | 2:112,942,805 | C/T | — | uncertain significance |
| rs759147714 | 2:112,942,831 | A/G | — | uncertain significance |
| rs374024290 | 2:112,942,841 | G/A | — | uncertain significance |
| rs2466838876 | 2:112,942,859 | T/C | — | uncertain significance |
| rs370895871 | 2:112,942,876 | G/A | — | uncertain significance |
| rs1683216817 | 2:112,942,882 | A/C | — | uncertain significance |
| rs757234528 | 2:112,944,722 | G/A | — | uncertain significance |
| rs143675954 | 2:112,944,853 | G/A | — | uncertain significance |
| rs768361747 | 2:112,944,869 | A/G | — | uncertain significance |
| rs1380238635 | 2:112,944,902 | G/C | — | uncertain significance |
| rs766235578 | 2:112,944,983 | C/T | — | uncertain significance |
| rs140094535 | 2:112,945,041 | C/T | — | likely benign |
| rs4848281 | 2:112,945,188 | T/G | — | — |
| rs72831633 | 2:112,945,932 | T/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.