ZNF600

zinc finger protein 600

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 Variants71 total

rsidPosition (GRCh37)AllelesClassClinVar
rs15055232219:53,268,880A/G—uncertain significance
rs75444938219:53,268,890A/G—uncertain significance
rs206256439219:53,268,965T/C—uncertain significance
rs74534661519:53,268,967A/T—uncertain significance
rs11712532919:53,268,990C/G—benign
rs75516254719:53,269,001C/A—uncertain significance
rs156862267919:53,269,073C/G—likely benign
rs37409867219:53,269,085T/C—likely benign
rs78140843619:53,269,112C/T—likely benign
rs251395365519:53,269,115G/A—uncertain significance
rs75285234119:53,269,129A/C—uncertain significance
rs76114248119:53,269,137T/G—uncertain significance
rs37376744019:53,269,205T/C—uncertain significance
rs14105473219:53,269,253C/T—uncertain significance
rs11302465119:53,269,255G/A—uncertain significance
rs13896180919:53,269,291C/T—uncertain significance
rs74774935219:53,269,346T/C—uncertain significance
rs76934923419:53,269,367G/T—uncertain significance
rs76111804819:53,269,384T/C—uncertain significance
rs20049011419:53,269,451G/A—uncertain significance
rs57157034019:53,269,458G/A—likely benign
rs251395651819:53,269,481T/A—uncertain significance
rs75686111519:53,269,502A/T—uncertain significance
rs141932525419:53,269,595A/T—uncertain significance
rs14242991419:53,269,619G/C—uncertain significance
rs14088976819:53,269,678T/G—uncertain significance
rs251395890619:53,269,761A/C—uncertain significance
rs36868981919:53,269,870T/G—uncertain significance
rs20186189219:53,269,882T/C—uncertain significance
rs19968415319:53,269,904G/C—uncertain significance
rs251396046419:53,269,921C/T—uncertain significance
rs11199323219:53,269,933T/C—benign
rs206258383919:53,270,006A/C—uncertain significance
rs77179140619:53,270,060G/T—uncertain significance
rs14929631819:53,270,071C/T—uncertain significance
rs75807351519:53,270,132G/A—uncertain significance
rs18833851719:53,270,135G/C—uncertain significance
rs76826043619:53,270,138G/A—uncertain significance
rs77583611619:53,270,188T/C—uncertain significance
rs11130124019:53,270,257C/T—benign
rs131467687519:53,270,284G/A—uncertain significance
rs18483021619:53,270,307T/C—likely benign
rs20209309119:53,270,349A/C—uncertain significance
rs57724293219:53,270,383C/T—uncertain significance
rs75545372619:53,270,393T/C—likely benign
rs251396488219:53,270,465T/C—uncertain significance
rs77202148519:53,270,509C/T—uncertain significance
rs14913210019:53,270,539A/G—uncertain significance
rs75752835019:53,270,552G/C—uncertain significance
rs14047574419:53,270,562G/C—benign
rs74695189319:53,270,578G/A—likely benign
rs77645659519:53,270,582A/G—uncertain significance
rs77293173119:53,270,593T/C—uncertain significance
rs76597018419:53,270,617G/A—uncertain significance
rs251396579219:53,270,619C/A—uncertain significance
rs11594894019:53,270,649C/T—benign
rs11623102719:53,270,692T/C—benign
rs37722580319:53,270,693T/C—uncertain significance
rs14442104819:53,270,696C/G—uncertain significance
rs14254985919:53,270,791T/C—uncertain significance
rs20170260219:53,270,817T/A—benign
rs11385257219:53,270,830A/G—uncertain significance
rs251396787719:53,270,918C/T—uncertain significance
rs54454817819:53,270,923A/G—uncertain significance
rs14682133019:53,270,926T/C—benign
rs144486816319:53,270,930A/G—likely benign
rs142326356319:53,270,936G/C—likely benign
rs56202398019:53,270,939A/G—likely benign
rs725281819:53,271,005T/C—benign
rs1040448619:53,284,135C/G——
rs650969419:53,338,671C/T——

Gene information from NCBI Gene. Variant classifications from ClinVar.