ZNF324B

zinc finger protein 324B

Summary

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA 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 Variants43 total

rsidPosition (GRCh37)AllelesClassClinVar
rs930481319:58,931,557A/Gdownstream gene variant
rs1167306919:58,934,918C/A
rs1297759219:58,961,056C/A
rs53826240619:58,963,622G/T
rs77939818619:58,965,148G/Auncertain significance
rs78053240819:58,965,672A/Glikely benign
rs75427621319:58,965,674G/Auncertain significance
rs251680854919:58,965,679T/Clikely benign
rs120244487719:58,965,701G/Tuncertain significance
rs74554557619:58,966,616C/Tuncertain significance
rs102130193719:58,966,624A/Cuncertain significance
rs37587348919:58,966,718C/Tuncertain significance
rs77132818719:58,966,730C/Tuncertain significance
rs20025314819:58,966,787G/Auncertain significance
rs76040018919:58,966,820A/Guncertain significance
rs75347847419:58,966,841A/Guncertain significance
rs206908928419:58,966,844C/Tuncertain significance
rs76246679819:58,966,934G/Cuncertain significance
rs126626754819:58,966,948C/Guncertain significance
rs251681466419:58,967,039G/Cuncertain significance
rs57196993319:58,967,110G/Auncertain significance
rs75535866219:58,967,118C/Guncertain significance
rs19983080019:58,967,186A/Cuncertain significance
rs120505175519:58,967,271G/Cuncertain significance
rs251681614419:58,967,318C/Tuncertain significance
rs75824577519:58,967,368G/Auncertain significance
rs36991033819:58,967,456C/Tuncertain significance
rs123859345519:58,967,512C/Tuncertain significance
rs75556147419:58,967,551T/Auncertain significance
rs251681748819:58,967,554C/Tuncertain significance
rs20010016719:58,967,593G/Cuncertain significance
rs76035745219:58,967,606G/Auncertain significance
rs89998523219:58,967,618G/Alikely benign
rs77941441419:58,967,627A/Guncertain significance
rs76048823719:58,967,693G/Clikely benign
rs37507397719:58,967,726G/Auncertain significance
rs91698031419:58,967,756T/Cuncertain significance
rs14188786819:58,967,760C/Tlikely benign
rs77763373719:58,967,782C/Tuncertain significance
rs19985873019:58,967,878C/Auncertain significance
rs77377526419:58,967,900G/Auncertain significance
rs156860624219:58,967,908G/Tuncertain significance
rs20135092219:58,967,927T/Cuncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.