ZNF276

zinc finger protein 276

Summary

Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in kinetochore. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants64 total

rsidPosition (GRCh37)AllelesClassClinVar
rs98495613016:89,788,053A/G—uncertain significance
rs93388069016:89,788,082C/G—uncertain significance
rs206128133016:89,788,085G/A—uncertain significance
rs120830771916:89,788,092C/G—uncertain significance
rs94518367016:89,788,101G/C—uncertain significance
rs75035115516:89,788,106G/A—uncertain significance
rs254392131316:89,788,134G/A—uncertain significance
rs90665313516:89,788,140G/C—uncertain significance
rs86735743116:89,788,154C/T—uncertain significance
rs100410940516:89,788,167C/G—uncertain significance
rs139146209416:89,788,201G/C—uncertain significance
rs53338978216:89,788,202G/T—uncertain significance
rs145285164416:89,788,212G/C—uncertain significance
rs215165846716:89,788,944G/C—uncertain significance
rs75456541216:89,789,032G/T—uncertain significance
rs91486828216:89,789,047G/C—uncertain significance
rs20215254416:89,789,049C/G—uncertain significance
rs117598255716:89,789,088C/T—uncertain significance
rs20033011516:89,789,173A/G—uncertain significance
rs116522314816:89,789,192C/A—uncertain significance
rs78000825416:89,789,209C/T—likely benign
rs19953025816:89,789,221G/A—uncertain significance
rs76366799616:89,789,235T/C—uncertain significance
rs74862428516:89,789,687C/A—uncertain significance
rs54332032416:89,789,703G/A—uncertain significance
rs137306006516:89,789,784T/C—uncertain significance
rs14992030416:89,789,840T/A—uncertain significance
rs128518719716:89,789,842C/T—uncertain significance
rs36763884216:89,789,907G/A—uncertain significance
rs76688481616:89,789,911C/T—uncertain significance
rs14776686116:89,789,920G/A—uncertain significance
rs20181082916:89,790,034C/G—uncertain significance
rs57347287316:89,790,057G/A—uncertain significance
rs6206838716:89,791,210C/T——
rs3502672616:89,791,279C/Tupstream gene variant—
rs1292502616:89,792,856C/Tintron variant—
rs75878138116:89,793,720C/A—uncertain significance
rs56519111916:89,793,721C/G—likely benign
rs1771924916:89,793,731C/T—likely benign
rs7280753916:89,794,051G/Aintron variant—
rs141123979516:89,795,648T/C—uncertain significance
rs37080478616:89,795,660A/G—uncertain significance
rs37303296416:89,795,693C/T—uncertain significance
rs19993090516:89,795,698G/A—uncertain significance
rs77577700116:89,795,723G/T—uncertain significance
rs3465964416:89,796,017G/C——
rs19039169016:89,796,581C/G——
rs37294079816:89,799,716T/C—likely benign
rs20012040616:89,799,725G/T—uncertain significance
rs128900611616:89,799,742C/T—uncertain significance
rs37742723816:89,799,792G/A—uncertain significance
rs37027744716:89,799,810C/T—uncertain significance
rs76953170216:89,799,913A/G—uncertain significance
rs75947908016:89,799,933A/C—uncertain significance
rs77918461116:89,799,942T/C—uncertain significance
rs14428151916:89,800,350G/A—uncertain significance
rs20205854516:89,800,359C/T—uncertain significance
rs120451722116:89,800,411G/A—uncertain significance
rs77653695316:89,804,276G/A—uncertain significance
rs78053230716:89,804,494G/A—uncertain significance
rs95186300216:89,804,561C/G—uncertain significance
rs74757157816:89,804,563A/T—uncertain significance
rs124054808216:89,804,565G/C—uncertain significance
rs5583033716:89,804,632C/T—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.