BEND4
BEN domain containing 4
Summary
Predicted to enable DNA binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs748010739 | 4:42,119,621 | C/G | — | uncertain significance |
| rs775677177 | 4:42,119,648 | G/A | — | uncertain significance |
| rs2475149230 | 4:42,119,674 | T/A | — | uncertain significance |
| rs73812731 | 4:42,119,721 | G/A | — | likely benign |
| rs2475149446 | 4:42,119,728 | G/C | — | uncertain significance |
| rs1560574798 | 4:42,122,106 | C/T | — | uncertain significance |
| rs779411414 | 4:42,122,161 | C/T | — | uncertain significance |
| rs374665634 | 4:42,122,185 | T/C | — | uncertain significance |
| rs1260231611 | 4:42,122,203 | T/A | — | uncertain significance |
| rs115737563 | 4:42,140,389 | T/A | intron variant | — |
| rs1469315221 | 4:42,145,519 | T/G | — | uncertain significance |
| rs145676520 | 4:42,145,534 | T/C | — | uncertain significance |
| rs552724030 | 4:42,145,544 | C/T | — | uncertain significance |
| rs202109836 | 4:42,145,639 | A/G | — | uncertain significance |
| rs191388972 | 4:42,145,649 | T/C | — | uncertain significance |
| rs1212277184 | 4:42,145,657 | G/A | — | uncertain significance |
| rs200251365 | 4:42,145,667 | C/G | — | uncertain significance |
| rs1193856877 | 4:42,145,675 | T/G | — | uncertain significance |
| rs754744473 | 4:42,145,696 | G/A | — | uncertain significance |
| rs139053577 | 4:42,145,827 | C/G | — | uncertain significance |
| rs1720979131 | 4:42,145,829 | G/C | — | uncertain significance |
| rs1461497103 | 4:42,145,865 | G/C | — | uncertain significance |
| rs374572332 | 4:42,145,873 | T/C | — | uncertain significance |
| rs777208498 | 4:42,145,886 | C/T | — | uncertain significance |
| rs191493014 | 4:42,145,924 | T/C | — | likely benign |
| rs200539776 | 4:42,145,969 | C/T | — | uncertain significance |
| rs200387125 | 4:42,146,005 | C/T | — | uncertain significance |
| rs6856819 | 4:42,150,213 | C/A | — | — |
| rs4501255 | 4:42,151,306 | C/G | intron variant | — |
| rs1241909580 | 4:42,153,686 | C/G | — | uncertain significance |
| rs932119677 | 4:42,153,709 | G/A | — | uncertain significance |
| rs1721292672 | 4:42,153,716 | C/A | — | uncertain significance |
| rs774751620 | 4:42,153,721 | C/G | — | uncertain significance |
| rs2475223398 | 4:42,153,742 | G/C | — | uncertain significance |
| rs1206229869 | 4:42,153,743 | G/T | — | uncertain significance |
| rs2475223491 | 4:42,153,766 | A/C | — | uncertain significance |
| rs2475223771 | 4:42,153,808 | T/G | — | likely benign |
| rs866025967 | 4:42,153,872 | C/G | — | uncertain significance |
| rs1221449413 | 4:42,153,887 | G/C | — | uncertain significance |
| rs569108834 | 4:42,153,893 | G/A | — | uncertain significance |
| rs1015497117 | 4:42,153,898 | G/A | — | uncertain significance |
| rs982070468 | 4:42,153,899 | G/C | — | uncertain significance |
| rs903419163 | 4:42,153,943 | C/A | — | uncertain significance |
| rs865971117 | 4:42,153,964 | G/A | — | uncertain significance |
| rs2475224560 | 4:42,153,967 | T/C | — | uncertain significance |
| rs1375938460 | 4:42,153,975 | G/C | — | uncertain significance |
| rs1471300349 | 4:42,153,980 | G/A | — | uncertain significance |
| rs767101355 | 4:42,153,997 | G/A | — | uncertain significance |
| rs1015821377 | 4:42,154,008 | G/T | — | uncertain significance |
| rs368416318 | 4:42,154,035 | C/T | — | likely benign |
| rs1260239906 | 4:42,154,063 | T/C | — | uncertain significance |
| rs1721320711 | 4:42,154,082 | G/A | — | uncertain significance |
| rs779302518 | 4:42,154,091 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.