ZNF225

zinc finger protein 225

Summary

Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants40 total

rsidPosition (GRCh37)AllelesClassClinVar
rs37066179319:44,620,002A/G—likely benign
rs76287342519:44,622,344G/A—conflicting classifications of pathogenicity
rs14754500019:44,622,413A/G—conflicting classifications of pathogenicity
rs137411045319:44,622,426G/A—likely benign
rs74580409919:44,622,638A/G—uncertain significance
rs75980985319:44,622,710A/G—uncertain significance
rs19054263819:44,631,026G/Aintron variant—
rs251441960219:44,635,038G/C—uncertain significance
rs75148898819:44,635,116T/G—uncertain significance
rs75494272919:44,635,120T/C—uncertain significance
rs18812715419:44,635,149G/C—uncertain significance
rs77253146419:44,635,188A/T—uncertain significance
rs76870548419:44,635,194G/A—likely benign
rs36807001319:44,635,257G/C—uncertain significance
rs37303353119:44,635,342G/A—uncertain significance
rs78116027519:44,635,408A/T—uncertain significance
rs36980952119:44,635,420A/G—uncertain significance
rs75329531219:44,635,659C/T—uncertain significance
rs36889050219:44,635,666G/C—uncertain significance
rs20022799519:44,635,702G/A—likely benign
rs37686622919:44,635,789A/G—uncertain significance
rs20173767319:44,635,899G/A—uncertain significance
rs19974046219:44,635,924G/A—uncertain significance
rs20037010119:44,636,010C/T—uncertain significance
rs76514235819:44,636,029C/G—uncertain significance
rs77958992819:44,636,043A/G—uncertain significance
rs145092760219:44,636,055T/C—uncertain significance
rs19137630419:44,636,131C/G—likely benign
rs78005554019:44,636,358C/T—uncertain significance
rs77289959019:44,636,364G/C—uncertain significance
rs37774592319:44,636,401G/A—uncertain significance
rs76860829419:44,636,455C/G—uncertain significance
rs20120212019:44,636,503G/A—likely benign
rs56980439419:44,636,622A/G—uncertain significance
rs120255718419:44,636,629A/G—uncertain significance
rs147952144719:44,636,646G/A—uncertain significance
rs75053705719:44,636,713A/T—uncertain significance
rs75622414719:44,636,734A/G—uncertain significance
rs75125183119:44,636,791G/A—uncertain significance
rs20109013919:44,636,857C/T—likely benign

Gene information from NCBI Gene. Variant classifications from ClinVar.