ZBTB24

zinc finger and BTB domain containing 24

Summary

Predicted to enable DNA-binding transcription factor activity 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 act upstream of or within hematopoietic progenitor cell differentiation. Predicted to be located in nucleus. Implicated in immunodeficiency-centromeric instability-facial anomalies syndrome 2. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants388 total

rsidPosition (GRCh37)AllelesClassClinVar
rs10469436:109,783,941A/T——
rs15542275746:109,787,054T/C—uncertain significance
rs12647089796:109,787,069G/C—likely benign
rs1467706596:109,787,070C/T—uncertain significance
rs1483539686:109,787,078C/T—likely benign
rs2017658216:109,787,079G/A—uncertain significance
rs7562606806:109,787,080T/C—uncertain significance
rs24828501926:109,787,082G/A—uncertain significance
rs24828502216:109,787,090C/T—likely benign
rs3733261766:109,787,092C/T—uncertain significance
rs7659482506:109,787,093G/A—likely benign
rs3739514786:109,787,096G/A—likely benign
rs2003780806:109,787,098G/A—uncertain significance
rs7754925986:109,787,107G/A—conflicting classifications of pathogenicity
rs1421896756:109,787,111C/T—likely benign
rs7763107416:109,787,112G/A—uncertain significance
rs21153529006:109,787,123C/G—uncertain significance
rs24828504796:109,787,130A/G—uncertain significance
rs7664962676:109,787,152C/T—uncertain significance
rs7779702636:109,787,162T/C—likely benign
rs7635322246:109,787,163G/A—uncertain significance
rs5746573856:109,787,164T/C—conflicting classifications of pathogenicity
rs7789434026:109,787,174G/C—likely benign
rs12227953166:109,787,179C/T—uncertain significance
rs24828506236:109,787,189C/T—likely benign
rs7474896106:109,787,192T/C—likely benign
rs7681901566:109,787,195A/G—likely benign
rs7761480696:109,787,199G/T—uncertain significance
rs7475598316:109,787,202T/C—uncertain significance
rs17760301376:109,787,212C/T—uncertain significance
rs7512428256:109,787,216T/C—likely benign
rs7547177086:109,787,223T/C—uncertain significance
rs7675153356:109,787,225G/A—likely benign
rs12306205776:109,787,240G/A—likely benign
rs24828509816:109,787,245C/T—uncertain significance
rs1458945396:109,787,255T/C—likely benign
rs12130624766:109,787,257G/C—uncertain significance
rs17760318036:109,787,259G/A—uncertain significance
rs21153530506:109,787,264C/T—likely benign
rs10305931446:109,787,281T/C—uncertain significance
rs3685289866:109,787,291G/A—likely benign
rs7729695446:109,787,292C/T—uncertain significance
rs7489194566:109,787,294C/G—uncertain significance
rs7706678266:109,787,299T/C—uncertain significance
rs1384934596:109,787,312C/T—likely benign
rs24828511786:109,787,318T/C—likely benign
rs15622989986:109,787,336A/G—likely benign
rs7675662926:109,787,337T/C—uncertain significance
rs24828512266:109,787,342C/A—likely benign
rs17760342376:109,787,344G/A—likely benign
rs3718309056:109,787,360C/T—likely benign
rs7652078656:109,787,361G/A—uncertain significance
rs17760347836:109,787,362T/C—uncertain significance
rs14585994476:109,787,363G/T—likely benign
rs17760350476:109,787,374G/A—uncertain significance
rs24828513566:109,787,381A/G—likely benign
rs12536542856:109,787,386G/T—uncertain significance
rs5770998586:109,787,393A/C—likely benign
rs17760356416:109,787,395T/A—uncertain significance
rs1394910746:109,787,398T/A—conflicting classifications of pathogenicity
rs12367096916:109,787,400T/C—uncertain significance
rs7553343026:109,787,402T/C—benign
rs7531270746:109,787,414T/C—likely benign
rs7487599216:109,787,420C/T—likely benign
rs12963135686:109,787,426G/A—likely benign
rs1397267596:109,787,433C/T—uncertain significance
rs1493794006:109,787,441A/T—likely benign
rs1447544536:109,787,446C/T—likely benign
rs22324496:109,787,447G/A—benign
rs7755475726:109,787,448G/C—uncertain significance
rs13442288066:109,787,459G/A—likely benign
rs1428301046:109,787,460A/G—conflicting classifications of pathogenicity
rs10259517786:109,787,462G/A—likely benign
rs21153532696:109,787,463T/G—uncertain significance
rs3699251426:109,787,465A/G—likely benign
rs12721925936:109,787,467G/A—uncertain significance
rs17760387926:109,787,472G/C—uncertain significance
rs617317366:109,787,476C/T—likely benign
rs7517705026:109,787,477G/A—likely benign
rs7781105736:109,787,482C/T—uncertain significance
rs5468723156:109,787,483G/A—likely benign
rs13963644076:109,787,506C/G—uncertain significance
rs5325632726:109,787,507C/T—likely benign
rs17760403616:109,787,519T/C—likely benign
rs13141690006:109,787,525T/A—likely benign
rs9634560926:109,787,527G/A—uncertain significance
rs7787644916:109,787,534C/G—uncertain significance
rs7454928946:109,787,546C/G—uncertain significance
rs7797418676:109,787,551C/G—uncertain significance
rs1873667346:109,787,555T/A—likely benign
rs7684896296:109,787,565C/T—uncertain significance
rs24828520506:109,787,591T/C—likely benign
rs10427626566:109,787,595G/C—uncertain significance
rs22324486:109,787,596C/T—benign
rs7746004166:109,787,610C/T—uncertain significance
rs13197010726:109,787,630C/T—likely benign
rs7610362776:109,787,647G/A—uncertain significance
rs2017251316:109,787,650C/A—uncertain significance
rs24828522206:109,787,660G/A—likely benign
rs24828522306:109,787,666C/T—likely benign

Showing 100 of 388 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.