ZNF341

zinc finger protein 341

Summary

Enables DNA binding activity and DNA-binding transcription activator activity. Predicted to be involved in regulation of DNA-templated transcription. Located in nucleus. Implicated in hyper IgE recurrent infection syndrome 3. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants501 total

rsidPosition (GRCh37)AllelesClassClinVar
rs53622689420:32,319,821C/T—benign
rs76220141720:32,319,833G/A—likely benign
rs125591414020:32,319,839G/A—likely benign
rs124246519720:32,319,847A/G—uncertain significance
rs116984821320:32,319,848G/A—likely benign
rs118307117620:32,319,855G/C—uncertain significance
rs20108540620:32,319,857G/A—uncertain significance
rs147836683220:32,319,858G/A—uncertain significance
rs141393629920:32,319,865G/C—likely benign
rs251543319620:32,319,867C/T—likely benign
rs88857022620:32,319,874G/A—likely benign
rs57612263620:32,319,875C/T—likely benign
rs116816171020:32,319,876C/T—likely benign
rs103663388720:32,319,877G/C—likely benign
rs228140220:32,319,894C/T—benign
rs57089044220:32,320,605G/T——
rs56373888820:32,323,083C/T——
rs36844558320:32,328,688G/A—likely benign
rs54213264420:32,328,696T/C—likely benign
rs212263495620:32,328,697T/C—likely benign
rs74538976320:32,328,717A/G—uncertain significance
rs77486420920:32,328,724C/T—likely benign
rs76204879620:32,328,725G/A—uncertain significance
rs133551745920:32,328,748G/A—likely benign
rs251544632620:32,328,766C/A—likely benign
rs53079667620:32,328,767C/T—uncertain significance
rs75971166820:32,328,774C/T—conflicting classifications of pathogenicity
rs37269075620:32,328,775G/A—likely benign
rs160123297320:32,328,787T/A—uncertain significance
rs15112059620:32,328,795C/T—uncertain significance
rs75132734520:32,328,796G/A—likely benign
rs19994789120:32,328,797C/T—uncertain significance
rs148067888720:32,328,798C/T—uncertain significance
rs78085715320:32,328,799C/G—likely benign
rs76713863320:32,332,891C/A—likely benign
rs37022016220:32,332,894C/T—likely benign
rs37204115320:32,332,895G/A—uncertain significance
rs7696360620:32,332,903C/T—benign
rs55651034120:32,332,913C/T—likely benign
rs57769901920:32,332,916G/T—benign
rs160123817320:32,332,922A/G—likely benign
rs75361466720:32,332,931C/T—likely benign
rs123786842220:32,332,932G/A—uncertain significance
rs212264501020:32,332,938T/G—uncertain significance
rs97013063120:32,332,946G/A—likely benign
rs126326772820:32,332,955C/T—likely benign
rs76297718620:32,332,957C/T—uncertain significance
rs20217538020:32,332,958G/A—likely benign
rs77420803320:32,332,961G/C—likely benign
rs120099653520:32,332,962C/T—uncertain significance
rs14047790020:32,332,966C/T—uncertain significance
rs18755723020:32,332,976C/T—likely benign
rs76597542820:32,332,983C/T—uncertain significance
rs54271593020:32,333,006C/T—likely benign
rs75207246720:32,333,007C/T—uncertain significance
rs14453385820:32,333,010G/A—benign
rs145331885920:32,333,021A/G—likely benign
rs77434581320:32,333,050C/T—uncertain significance
rs76167762420:32,333,056C/T—uncertain significance
rs14110661620:32,333,057G/A—likely benign
rs53195599320:32,333,071C/T—likely benign
rs20103769720:32,333,072G/A—likely benign
rs251545239420:32,333,081G/T—uncertain significance
rs143315345220:32,333,084C/T—likely benign
rs139424380620:32,333,085C/T—uncertain significance
rs90916503320:32,333,086C/T—uncertain significance
rs37374467320:32,333,094G/A—uncertain significance
rs53458582820:32,333,098A/G—uncertain significance
rs119474650220:32,333,100C/T—uncertain significance
rs37673818520:32,333,101G/A—uncertain significance
rs78029469520:32,333,112G/T—likely benign
rs727481120:32,333,181G/Tintron variantbenign
rs14237370820:32,336,709C/G—likely benign
rs212265376420:32,336,710T/C—likely benign
rs37582463520:32,336,713C/T—likely benign
rs251545781520:32,336,720A/T—likely benign
rs76671617820:32,336,721C/A—likely benign
rs75511197220:32,336,730T/A—uncertain significance
rs36887331120:32,336,736C/G—uncertain significance
rs140579553420:32,336,740C/T—likely benign
rs119786075120:32,336,752C/T—likely benign
rs123631872320:32,336,754C/T—uncertain significance
rs7594624320:32,336,755G/T—likely benign
rs18579586220:32,336,776G/A—likely benign
rs77091462320:32,336,781A/C—uncertain significance
rs251545800420:32,336,802A/G—uncertain significance
rs102704659220:32,336,806T/C—likely benign
rs14648554820:32,336,809G/A—likely benign
rs121781163320:32,336,810C/A—uncertain significance
rs54068718920:32,336,813A/C—uncertain significance
rs36789475920:32,336,821C/T—likely benign
rs102240255720:32,336,828G/A—uncertain significance
rs133081929420:32,336,838C/T—uncertain significance
rs37174702820:32,336,856C/A—uncertain significance
rs14344400620:32,336,857C/T—likely benign
rs97832678220:32,336,861G/T—uncertain significance
rs143929231720:32,336,867C/T—uncertain significance
rs14101730720:32,336,868C/G—uncertain significance
rs77526482620:32,336,870C/T—uncertain significance
rs76842347420:32,336,887G/A—likely benign

Showing 100 of 501 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.