ZRANB3
zinc finger RANBP2-type containing 3
Summary
Enables ATP-dependent DNA/DNA annealing activity; DNA endonuclease activity; and K63-linked polyubiquitin modification-dependent protein binding activity. Involved in DNA repair; replication fork reversal; and response to UV. Located in nuclear replication fork and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs755703444 | 2:135,957,974 | T/C | — | uncertain significance |
| rs2468327845 | 2:135,960,532 | A/G | — | uncertain significance |
| rs6721694 | 2:135,965,002 | A/G | — | benign |
| rs746835208 | 2:135,965,089 | A/T | — | uncertain significance |
| rs1273911618 | 2:135,965,185 | T/C | — | uncertain significance |
| rs769887849 | 2:135,965,230 | G/A | — | likely benign |
| rs753033293 | 2:135,965,263 | T/A | — | uncertain significance |
| rs114791090 | 2:135,965,272 | C/A | — | uncertain significance |
| rs2468335709 | 2:135,965,320 | T/C | — | uncertain significance |
| rs2468335984 | 2:135,965,365 | G/A | — | uncertain significance |
| rs765400604 | 2:135,965,377 | G/A | — | uncertain significance |
| rs777825209 | 2:135,965,394 | T/G | — | uncertain significance |
| rs1693987415 | 2:135,966,464 | C/G | — | uncertain significance |
| rs2468337812 | 2:135,966,528 | A/T | — | uncertain significance |
| rs779621882 | 2:135,975,095 | C/T | — | uncertain significance |
| rs774807770 | 2:135,976,654 | C/T | — | uncertain significance |
| rs1211413604 | 2:135,976,655 | G/A | — | uncertain significance |
| rs374940077 | 2:135,976,688 | C/A | — | uncertain significance |
| rs1573693336 | 2:135,976,719 | A/T | — | likely benign |
| rs369602423 | 2:135,976,726 | T/C | — | uncertain significance |
| rs200511870 | 2:135,982,016 | G/A | — | uncertain significance |
| rs370147456 | 2:135,982,024 | T/C | — | uncertain significance |
| rs902594500 | 2:135,985,396 | G/C | — | uncertain significance |
| rs1334264785 | 2:135,985,463 | C/G | — | uncertain significance |
| rs368267667 | 2:135,985,486 | T/G | — | uncertain significance |
| rs2468368386 | 2:135,985,570 | C/T | — | uncertain significance |
| rs753387351 | 2:135,988,142 | T/C | — | uncertain significance |
| rs756757933 | 2:135,988,145 | G/A | — | uncertain significance |
| rs778606468 | 2:135,988,157 | C/T | — | uncertain significance |
| rs61732190 | 2:135,988,224 | C/T | — | benign |
| rs75794892 | 2:135,988,282 | G/A | — | benign |
| rs576763166 | 2:135,988,289 | G/A | — | uncertain significance |
| rs2468373351 | 2:135,988,330 | A/C | — | uncertain significance |
| rs199511562 | 2:135,988,346 | A/C | — | uncertain significance |
| rs533207419 | 2:135,988,355 | G/A | — | uncertain significance |
| rs561345821 | 2:135,988,386 | C/T | — | uncertain significance |
| rs753002480 | 2:135,988,401 | G/A | — | uncertain significance |
| rs373989017 | 2:135,988,494 | C/T | — | uncertain significance |
| rs12471508 | 2:135,995,073 | G/A | — | — |
| rs1465146591 | 2:136,019,729 | C/A | — | — |
| rs202055620 | 2:136,023,192 | T/G | — | uncertain significance |
| rs1326584676 | 2:136,023,217 | T/C | — | uncertain significance |
| rs552765988 | 2:136,026,581 | A/G | — | uncertain significance |
| rs146966998 | 2:136,026,629 | C/T | — | uncertain significance |
| rs750230244 | 2:136,026,650 | T/C | — | uncertain significance |
| rs761870751 | 2:136,029,372 | C/T | — | uncertain significance |
| rs1436352558 | 2:136,029,373 | G/A | — | uncertain significance |
| rs2468453955 | 2:136,033,217 | T/C | — | uncertain significance |
| rs1266555586 | 2:136,033,232 | A/G | — | uncertain significance |
| rs7572152 | 2:136,068,890 | C/G | intron variant | — |
| rs531204874 | 2:136,073,062 | G/T | — | uncertain significance |
| rs1685126513 | 2:136,107,577 | G/A | — | uncertain significance |
| rs555044883 | 2:136,107,598 | C/T | — | uncertain significance |
| rs557903085 | 2:136,107,640 | G/A | — | uncertain significance |
| rs2468587816 | 2:136,107,732 | T/C | — | uncertain significance |
| rs61744517 | 2:136,107,757 | G/C | — | uncertain significance |
| rs955624524 | 2:136,111,090 | C/T | — | uncertain significance |
| rs2468593601 | 2:136,111,120 | G/C | — | uncertain significance |
| rs2468593617 | 2:136,111,125 | A/G | — | uncertain significance |
| rs572388412 | 2:136,111,129 | T/C | — | uncertain significance |
| rs761356826 | 2:136,111,130 | T/A | — | uncertain significance |
| rs3940549 | 2:136,138,627 | A/G | intron variant | — |
| rs6709525 | 2:136,161,092 | C/A | — | — |
| rs13384711 | 2:136,176,540 | T/A | — | — |
| rs4954256 | 2:136,187,252 | T/C | intron variant | — |
| rs10209482 | 2:136,191,314 | A/C | intron variant | — |
| rs776958301 | 2:136,261,917 | G/A | — | uncertain significance |
| rs6735329 | 2:136,273,578 | T/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.