ZNF611

zinc finger protein 611

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 Variants59 total

rsidPosition (GRCh37)AllelesClassClinVar
rs36973667719:53,208,225G/Auncertain significance
rs206222955419:53,208,257C/Tuncertain significance
rs76173450819:53,208,279G/Auncertain significance
rs14786626519:53,208,353C/Auncertain significance
rs36801212219:53,208,387G/Auncertain significance
rs14082079919:53,208,404G/Auncertain significance
rs76984288319:53,208,413C/Tuncertain significance
rs14865577319:53,208,414G/Auncertain significance
rs251514175019:53,208,439C/Auncertain significance
rs14556878119:53,208,494C/Tuncertain significance
rs20113031119:53,208,495G/Auncertain significance
rs117038122719:53,208,606A/Cuncertain significance
rs20056557219:53,208,671G/Cuncertain significance
rs251514316219:53,208,720T/Cuncertain significance
rs76517520719:53,208,746C/Tuncertain significance
rs251514404619:53,208,870T/Cuncertain significance
rs19969920519:53,208,882C/Tuncertain significance
rs123972763319:53,208,953T/Guncertain significance
rs13920654319:53,209,064C/Tuncertain significance
rs37309239219:53,209,085G/Alikely benign
rs147759111719:53,209,107T/Cuncertain significance
rs251514535319:53,209,151T/Cuncertain significance
rs76920324919:53,209,178T/Cuncertain significance
rs125528262019:53,209,202G/Cuncertain significance
rs76239401319:53,209,214G/Cuncertain significance
rs7621081019:53,209,215T/Cuncertain significance
rs74605200419:53,209,251T/Guncertain significance
rs92245413219:53,209,268T/Cuncertain significance
rs74700231919:53,209,280T/Cuncertain significance
rs20020215619:53,209,350A/Guncertain significance
rs128627786519:53,209,361T/Guncertain significance
rs13844729119:53,209,412T/Guncertain significance
rs74546381719:53,209,418C/Tuncertain significance
rs75983530319:53,209,475T/Cuncertain significance
rs76776077219:53,209,476C/Guncertain significance
rs156859992019:53,209,493T/Cuncertain significance
rs76411960519:53,209,497C/Tlikely benign
rs13921799119:53,209,514C/Auncertain significance
rs11304664319:53,209,575G/Cuncertain significance
rs56746792919:53,209,709G/Auncertain significance
rs14633768119:53,209,712C/Tuncertain significance
rs75927080119:53,209,800A/Tuncertain significance
rs122981105419:53,209,823G/Auncertain significance
rs20197368419:53,209,937C/Tuncertain significance
rs251514899419:53,209,991A/Cuncertain significance
rs14912350719:53,209,993T/Glikely benign
rs77541182219:53,210,063G/Cuncertain significance
rs251514933419:53,210,064T/Auncertain significance
rs36894937119:53,210,088C/Auncertain significance
rs131271201119:53,217,294T/Guncertain significance
rs14709961419:53,217,328A/Clikely benign
rs139529153319:53,217,340A/Tuncertain significance
rs76917396519:53,217,357G/Auncertain significance
rs76545417919:53,217,367T/Cuncertain significance
rs77363697719:53,217,376C/Tuncertain significance
rs254795019:53,217,906C/G
rs129382943419:53,219,119C/Tuncertain significance
rs37151468319:53,219,135C/Tuncertain significance
rs726029319:53,229,394C/Tregulatory region variant

Gene information from NCBI Gene. Variant classifications from ClinVar.