BAHD1

bromo adjacent homology domain containing 1

Summary

Enables chromatin binding activity. Involved in heterochromatin formation and negative regulation of DNA-templated transcription. Located in nucleoplasm. Part of chromatin silencing complex. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants57 total

rsidPosition (GRCh37)AllelesClassClinVar
rs54942603315:40,730,284G/A
rs14519153515:40,750,746G/Auncertain significance
rs77511883015:40,750,763G/Auncertain significance
rs76386984115:40,750,818G/Auncertain significance
rs37565952215:40,750,987C/Auncertain significance
rs159585872615:40,751,031A/Guncertain significance
rs37519275415:40,751,093C/Tuncertain significance
rs75006020315:40,751,094G/Auncertain significance
rs36939777215:40,751,120C/Tuncertain significance
rs138392235715:40,751,124G/Auncertain significance
rs37761197815:40,751,127G/Auncertain significance
rs77440192215:40,751,130A/Tuncertain significance
rs20003721415:40,751,178G/Auncertain significance
rs37432159515:40,751,204C/Tuncertain significance
rs76470313215:40,751,205G/Auncertain significance
rs37416118415:40,751,241C/Tuncertain significance
rs20060108715:40,751,247G/Auncertain significance
rs75383004315:40,751,343G/Auncertain significance
rs13788908915:40,751,381C/Guncertain significance
rs14269394515:40,751,403C/Guncertain significance
rs37256626815:40,751,526C/Auncertain significance
rs380335715:40,751,555C/Abenign
rs254295888515:40,751,577A/Guncertain significance
rs15062321415:40,751,594C/Tuncertain significance
rs77432330415:40,751,645C/Tuncertain significance
rs103495926415:40,751,724C/Tuncertain significance
rs75542106415:40,751,855A/Guncertain significance
rs97293007715:40,751,888G/Auncertain significance
rs20210399215:40,751,889C/Tuncertain significance
rs254296269215:40,751,954C/Auncertain significance
rs19950020915:40,751,987G/Auncertain significance
rs74940026215:40,751,991A/Guncertain significance
rs13875934515:40,752,020G/Auncertain significance
rs14184594715:40,752,065G/Auncertain significance
rs76506774615:40,754,176G/Cuncertain significance
rs138509765915:40,754,182C/Guncertain significance
rs189405788715:40,754,186T/Auncertain significance
rs189405825615:40,754,189T/Auncertain significance
rs75894837715:40,754,230G/Auncertain significance
rs14959591415:40,754,245A/Guncertain significance
rs20033672315:40,754,255C/Tuncertain significance
rs104070378415:40,754,272G/Cuncertain significance
rs124291740215:40,754,276G/Auncertain significance
rs74964860015:40,754,279C/Guncertain significance
rs97363429815:40,754,342G/Cuncertain significance
rs74820929515:40,754,350A/Guncertain significance
rs254297430015:40,754,360G/Cuncertain significance
rs54620462415:40,754,389A/Cuncertain significance
rs56319148615:40,754,408G/Auncertain significance
rs37380097015:40,754,425C/Tuncertain significance
rs76939180615:40,754,428C/Tuncertain significance
rs14300730915:40,754,435G/Auncertain significance
rs20194573315:40,756,088G/Auncertain significance
rs254298560515:40,756,718A/Cuncertain significance
rs103898492415:40,757,599G/Tuncertain significance
rs254299343215:40,758,243C/Guncertain significance
rs74546535915:40,758,284T/Auncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.