BACH2

BACH transcriptional regulator 2

Summary

Enables sequence-specific double-stranded DNA binding activity. Involved in primary adaptive immune response involving T cells and B cells. Located in cytosol and nucleoplasm. Part of RNA polymerase II transcription regulator complex. Implicated in immunodeficiency 60. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants435 total

rsidPosition (GRCh37)AllelesClassClinVar
rs22895776:90,640,491C/T3 prime UTR variant—
rs2001660946:90,642,117A/T—benign
rs3696883226:90,642,120C/T—likely benign
rs7512118416:90,642,131G/C—uncertain significance
rs12463175796:90,642,133A/G—likely benign
rs25335368036:90,642,142C/T—likely benign
rs25335368216:90,642,148C/T—likely benign
rs5362629076:90,642,154G/A—likely benign
rs21283523026:90,642,172A/T—likely benign
rs25335368696:90,642,184G/A—likely benign
rs1422543036:90,642,195C/G—uncertain significance
rs1388008506:90,642,196G/A—likely benign
rs7723007526:90,642,208G/A—likely benign
rs21283523176:90,642,225G/A—uncertain significance
rs25335369706:90,642,229T/C—likely benign
rs1419768546:90,642,235C/G—likely benign
rs25335370656:90,642,237C/G—uncertain significance
rs9686474996:90,642,242A/G—uncertain significance
rs3734372226:90,642,250C/T—likely benign
rs2013595876:90,642,251G/A—uncertain significance
rs12444490766:90,642,261C/A—uncertain significance
rs3710784426:90,642,267G/C—uncertain significance
rs14720372496:90,642,268T/C—likely benign
rs7542992076:90,642,287T/G—uncertain significance
rs7576529956:90,642,291C/T—uncertain significance
rs786882366:90,642,292G/A—benign
rs14693172596:90,642,313G/A—likely benign
rs17727263596:90,642,314G/A—uncertain significance
rs7507058616:90,642,315G/A—uncertain significance
rs1889270206:90,642,316G/T—likely benign
rs13929830136:90,642,318G/A—uncertain significance
rs2005057766:90,642,319T/C—likely benign
rs7686106886:90,642,321C/T—uncertain significance
rs1396274626:90,642,322G/A—likely benign
rs1996465826:90,642,326G/A—uncertain significance
rs2006710836:90,642,327G/T—uncertain significance
rs17727303706:90,642,330C/T—uncertain significance
rs1412316786:90,642,331C/T—likely benign
rs3751033806:90,642,332G/A—uncertain significance
rs7603008046:90,642,333C/T—uncertain significance
rs1507715216:90,642,334G/A—likely benign
rs3684168316:90,642,338G/A—uncertain significance
rs7667722256:90,642,345A/G—likely benign
rs25335374046:90,642,347C/T—uncertain significance
rs17727335446:90,642,352G/C—likely benign
rs7551008356:90,642,357C/T—uncertain significance
rs37987896:90,642,358A/G—benign
rs13457331306:90,642,359T/C—uncertain significance
rs7492825546:90,642,364C/T—likely benign
rs3746200736:90,642,372C/A—uncertain significance
rs3686526706:90,642,373G/A—likely benign
rs9153216306:90,642,376T/C—likely benign
rs7760409806:90,642,385C/T—likely benign
rs7613636276:90,642,386G/A—uncertain significance
rs11710976196:90,642,390T/G—likely benign
rs10425231476:90,642,400A/C—likely benign
rs1476493266:90,642,412C/T—likely benign
rs1402704406:90,642,413G/A—uncertain significance
rs7677488836:90,642,418G/A—likely benign
rs13216998646:90,642,423T/C—uncertain significance
rs14071014026:90,642,425C/G—uncertain significance
rs12913763926:90,642,431G/A—uncertain significance
rs1479088286:90,642,433C/T—likely benign
rs12955564166:90,642,436G/A—likely benign
rs13591025086:90,642,450G/A—uncertain significance
rs12448602686:90,642,454G/C—likely benign
rs1477872946:90,642,462G/A—uncertain significance
rs7467842026:90,642,463G/A—likely benign
rs3748121576:90,642,470C/T—uncertain significance
rs7808834036:90,642,471G/A—uncertain significance
rs25335377286:90,642,478G/T—likely benign
rs13465713726:90,642,492C/T—uncertain significance
rs729239046:90,642,493A/G—benign
rs1931233066:90,642,495G/T—likely benign
rs17727536926:90,642,502G/C—uncertain significance
rs7746198076:90,642,509C/T—uncertain significance
rs25335378326:90,642,517T/C—likely benign
rs7736197766:90,642,521T/C—uncertain significance
rs25335378606:90,642,546A/G—likely benign
rs1165886816:90,642,550T/C—benign
rs7513684016:90,642,605C/T—uncertain significance
rs25335379536:90,642,613G/A—likely benign
rs3732383496:90,642,616A/G—likely benign
rs3775097426:90,642,620G/A—likely benign
rs1823826:90,647,759G/C—benign
rs7618638756:90,647,852G/A—likely benign
rs7514473026:90,647,855C/T—likely benign
rs13314000386:90,647,867T/C—uncertain significance
rs7547411426:90,647,870C/T—uncertain significance
rs7809895536:90,647,879C/T—uncertain significance
rs7524316116:90,647,887A/G—likely benign
rs25335459146:90,647,909C/T—uncertain significance
rs25335459206:90,647,912T/C—uncertain significance
rs21283538136:90,647,914G/A—likely benign
rs3716954256:90,647,926G/A—likely benign
rs7775472196:90,647,929C/T—likely benign
rs25335459646:90,647,936C/A—uncertain significance
rs11565884546:90,647,958C/T—uncertain significance
rs25335460396:90,647,961C/T—uncertain significance
rs1510852826:90,647,962A/G—likely benign

Showing 100 of 435 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.