ZNF268
zinc finger protein 268
Summary
Predicted to enable DNA binding activity and DNA-binding transcription factor activity. Involved in several processes, including positive regulation of non-canonical NF-kappaB signal transduction; regulation of apoptotic process; and regulation of primary metabolic process. Located in cytosol and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs572005987 | 12:133,758,594 | G/C | — | uncertain significance |
| rs201717119 | 12:133,758,612 | T/C | — | uncertain significance |
| rs2500707286 | 12:133,764,641 | A/G | — | uncertain significance |
| rs775444456 | 12:133,768,091 | T/C | — | uncertain significance |
| rs778532742 | 12:133,768,538 | G/A | — | uncertain significance |
| rs1239872544 | 12:133,768,550 | T/C | — | uncertain significance |
| rs540763931 | 12:133,768,573 | A/G | — | likely benign |
| rs12305809 | 12:133,777,466 | A/G | intron variant | — |
| rs61960706 | 12:133,777,822 | G/A | intron variant | — |
| rs141714051 | 12:133,778,777 | A/G | — | uncertain significance |
| rs375049594 | 12:133,778,797 | G/A | — | likely benign |
| rs779561505 | 12:133,778,812 | A/G | — | likely benign |
| rs774816435 | 12:133,778,865 | A/G | — | uncertain significance |
| rs779550814 | 12:133,778,934 | G/T | — | uncertain significance |
| rs2500775552 | 12:133,778,960 | C/A | — | uncertain significance |
| rs199759939 | 12:133,778,969 | T/C | — | uncertain significance |
| rs1014058483 | 12:133,779,051 | A/G | — | uncertain significance |
| rs373015628 | 12:133,779,089 | G/A | — | uncertain significance |
| rs769424497 | 12:133,779,111 | G/A | — | likely benign |
| rs1242726379 | 12:133,779,170 | G/A | — | uncertain significance |
| rs746814708 | 12:133,779,229 | C/T | — | likely benign |
| rs201735332 | 12:133,779,285 | G/A | — | uncertain significance |
| rs377566580 | 12:133,779,371 | A/G | — | uncertain significance |
| rs199607782 | 12:133,779,423 | G/A | — | uncertain significance |
| rs2500778869 | 12:133,779,432 | C/T | — | uncertain significance |
| rs2500779111 | 12:133,779,488 | C/T | — | uncertain significance |
| rs371484741 | 12:133,779,518 | T/A | — | uncertain significance |
| rs567462605 | 12:133,779,564 | T/G | — | uncertain significance |
| rs374317261 | 12:133,779,585 | A/G | — | uncertain significance |
| rs372811790 | 12:133,779,633 | C/T | — | uncertain significance |
| rs1956795236 | 12:133,779,666 | T/C | — | uncertain significance |
| rs369587420 | 12:133,779,750 | G/A | — | uncertain significance |
| rs536753332 | 12:133,779,763 | G/T | — | uncertain significance |
| rs1956803281 | 12:133,779,902 | A/C | — | uncertain significance |
| rs765014090 | 12:133,779,953 | T/C | — | uncertain significance |
| rs1435883657 | 12:133,779,959 | A/G | — | uncertain significance |
| rs764011877 | 12:133,780,146 | C/T | — | uncertain significance |
| rs779612954 | 12:133,780,187 | C/T | — | uncertain significance |
| rs566079280 | 12:133,780,221 | C/T | — | uncertain significance |
| rs2500783663 | 12:133,780,238 | A/G | — | uncertain significance |
| rs370704179 | 12:133,780,239 | T/C | — | uncertain significance |
| rs373847832 | 12:133,780,250 | G/C | — | uncertain significance |
| rs1956816023 | 12:133,780,251 | G/A | — | likely benign |
| rs36127550 | 12:133,780,309 | G/T | — | benign |
| rs368574793 | 12:133,780,320 | T/C | — | uncertain significance |
| rs887159304 | 12:133,780,328 | C/T | — | uncertain significance |
| rs577089058 | 12:133,780,390 | G/C | — | uncertain significance |
| rs758752286 | 12:133,780,397 | T/G | — | uncertain significance |
| rs778328447 | 12:133,780,400 | T/C | — | uncertain significance |
| rs2500784735 | 12:133,780,421 | A/G | — | uncertain significance |
| rs757743538 | 12:133,780,535 | A/C | — | uncertain significance |
| rs372113417 | 12:133,780,559 | A/G | — | uncertain significance |
| rs373286359 | 12:133,780,587 | G/A | — | uncertain significance |
| rs1566386611 | 12:133,780,622 | G/C | — | uncertain significance |
| rs570108006 | 12:133,780,667 | A/G | — | uncertain significance |
| rs1956835223 | 12:133,780,691 | C/T | — | uncertain significance |
| rs755132414 | 12:133,780,709 | T/C | — | uncertain significance |
| rs758836562 | 12:133,780,755 | G/A | — | uncertain significance |
| rs2500787134 | 12:133,780,769 | G/T | — | uncertain significance |
| rs750819157 | 12:133,780,833 | A/G | — | uncertain significance |
| rs1048619959 | 12:133,780,841 | A/G | — | uncertain significance |
| rs908827082 | 12:133,780,847 | A/G | — | uncertain significance |
| rs2500788065 | 12:133,780,887 | C/T | — | uncertain significance |
| rs536275352 | 12:133,780,902 | C/T | — | uncertain significance |
| rs771733109 | 12:133,780,960 | A/C | — | uncertain significance |
| rs996071782 | 12:133,781,088 | A/G | — | uncertain significance |
| rs771680209 | 12:133,781,106 | A/G | — | uncertain significance |
| rs36174733 | 12:133,781,163 | A/G | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.