BEND7
BEN domain containing 7
Summary
Predicted to enable DNA binding activity. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1835050512 | 10:13,481,194 | T/G | — | uncertain significance |
| rs758072709 | 10:13,481,252 | G/A | — | uncertain significance |
| rs751077006 | 10:13,481,369 | G/A | — | uncertain significance |
| rs2538801494 | 10:13,481,431 | C/T | — | likely benign |
| rs2130773287 | 10:13,481,471 | G/T | — | uncertain significance |
| rs112746362 | 10:13,481,477 | T/C | — | uncertain significance |
| rs377375734 | 10:13,489,310 | G/A | — | uncertain significance |
| rs762817498 | 10:13,494,637 | G/T | — | uncertain significance |
| rs7096540 | 10:13,495,241 | T/C | intron variant | — |
| rs10906376 | 10:13,499,253 | C/A | intron variant | — |
| rs374073381 | 10:13,522,946 | T/C | — | uncertain significance |
| rs2539769561 | 10:13,522,954 | T/G | — | uncertain significance |
| rs2539772058 | 10:13,523,012 | C/G | — | uncertain significance |
| rs746041860 | 10:13,523,046 | G/A | — | uncertain significance |
| rs371441138 | 10:13,523,052 | A/G | — | uncertain significance |
| rs17153352 | 10:13,530,217 | T/A | intron variant | — |
| rs11258417 | 10:13,533,053 | C/T | intron variant | — |
| rs764666615 | 10:13,534,649 | G/C | — | uncertain significance |
| rs34031551 | 10:13,534,655 | G/A | — | uncertain significance |
| rs2540038695 | 10:13,534,684 | G/C | — | uncertain significance |
| rs761261458 | 10:13,534,718 | A/C | — | likely benign |
| rs144230873 | 10:13,534,766 | G/A | — | uncertain significance |
| rs7921105 | 10:13,535,398 | C/T | intron variant | — |
| rs776950071 | 10:13,538,791 | C/T | — | uncertain significance |
| rs201032751 | 10:13,538,826 | T/C | — | uncertain significance |
| rs1468885400 | 10:13,541,820 | T/C | — | uncertain significance |
| rs779256777 | 10:13,541,864 | G/C | — | uncertain significance |
| rs140777387 | 10:13,541,886 | G/A | — | uncertain significance |
| rs147003029 | 10:13,541,912 | G/T | — | uncertain significance |
| rs745972440 | 10:13,542,011 | C/T | — | uncertain significance |
| rs761673353 | 10:13,542,056 | T/C | — | uncertain significance |
| rs7075477 | 10:13,544,285 | A/C | intron variant | — |
| rs61833902 | 10:13,547,405 | C/T | upstream gene variant | — |
| rs10160101 | 10:13,549,462 | G/C | upstream gene variant | — |
| rs11258435 | 10:13,568,857 | T/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.