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

Gene information from NCBI Gene. Variant classifications from ClinVar.