ZSCAN1

zinc finger and SCAN domain containing 1

Summary

Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants38 total

rsidPosition (GRCh37)AllelesClassClinVar
rs75461538719:58,549,214C/Tuncertain significance
rs55741319919:58,549,241C/Tuncertain significance
rs93407144219:58,549,274G/Auncertain significance
rs118098415419:58,549,283G/Auncertain significance
rs37340595419:58,549,328C/Tuncertain significance
rs11337442219:58,549,354T/Cuncertain significance
rs7646338419:58,549,372G/Abenign
rs36985946419:58,549,395G/Tuncertain significance
rs251500917919:58,549,398A/Tuncertain significance
rs124568192219:58,549,416C/Tuncertain significance
rs75000585219:58,549,495G/Tuncertain significance
rs37624768819:58,549,514C/Guncertain significance
rs74836773519:58,549,519C/Guncertain significance
rs207375470119:58,549,561G/Auncertain significance
rs20198217019:58,551,836C/Tuncertain significance
rs75747473519:58,551,851A/Guncertain significance
rs13946184119:58,551,862G/Cuncertain significance
rs76944063819:58,551,904C/Tuncertain significance
rs54689626019:58,556,914A/Gcoding sequence variant
rs37204864319:58,563,961C/Tuncertain significance
rs77541333719:58,563,981G/Auncertain significance
rs77463246119:58,564,802C/Tuncertain significance
rs76068736019:58,564,803G/Auncertain significance
rs142687061719:58,564,961C/Guncertain significance
rs14449496519:58,564,967G/Auncertain significance
rs90335641919:58,564,995C/Auncertain significance
rs14574343119:58,565,043G/Auncertain significance
rs77728975919:58,565,063C/Tuncertain significance
rs74794389419:58,565,135C/Tuncertain significance
rs14317552019:58,565,154C/Tuncertain significance
rs37006684519:58,565,187A/Glikely benign
rs37166657219:58,565,228C/Guncertain significance
rs37593064219:58,565,232C/Tuncertain significance
rs20019073619:58,565,250G/Auncertain significance
rs36954701319:58,565,273G/Auncertain significance
rs207387589219:58,565,297G/Auncertain significance
rs142995581519:58,565,403C/Tlikely benign
rs54396522119:58,565,405C/Auncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.