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

Gene information from NCBI Gene. Variant classifications from ClinVar.