UGT2B4

UDP glucuronosyltransferase family 2 member B4

Summary

Enables glucuronosyltransferase activity. Involved in estrogen metabolic process and xenobiotic metabolic process. Predicted to be located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants57 total

rsidPosition (GRCh37)AllelesClassClinVar
rs3739083534:70,346,367C/Guncertain significance
rs25300107974:70,346,429C/Tuncertain significance
rs13990023414:70,346,443G/Auncertain significance
rs2002802024:70,346,480G/Astop gained
rs7783786494:70,346,510G/Auncertain significance
rs7457808264:70,346,553G/Tuncertain significance
rs5501520164:70,346,554A/Tuncertain significance
rs1846473684:70,346,581G/Auncertain significance
rs5586072624:70,346,588C/Guncertain significance
rs3684574834:70,346,621C/Tuncertain significance
rs725527064:70,350,950A/Guncertain significance
rs1809820404:70,350,974G/Cuncertain significance
rs7603932084:70,351,002C/Tuncertain significance
rs412974314:70,351,024T/Abenign
rs25300207574:70,351,098T/Cuncertain significance
rs1888619314:70,352,356T/Cuncertain significance
rs131111344:70,354,811G/Aintron variant
rs7759124614:70,355,169C/Auncertain significance
rs7632637234:70,355,173G/Cuncertain significance
rs7577283394:70,355,200C/Auncertain significance
rs25300304924:70,355,283C/Tuncertain significance
rs7460206674:70,359,437A/Guncertain significance
rs7513502844:70,359,439T/Auncertain significance
rs413000044:70,359,452C/Auncertain significance
rs25300380014:70,359,497A/Guncertain significance
rs17280653574:70,359,516T/Cuncertain significance
rs7674091194:70,359,544A/Guncertain significance
rs12815167504:70,359,547G/Auncertain significance
rs1453616674:70,360,904T/Auncertain significance
rs1854958304:70,360,912C/Alikely benign
rs14297112274:70,360,937T/Auncertain significance
rs15604361094:70,360,951C/Guncertain significance
rs25300409744:70,360,970G/Tuncertain significance
rs7804641184:70,360,985A/Cuncertain significance
rs17281167944:70,360,993A/Guncertain significance
rs7476256584:70,361,002T/Cuncertain significance
rs3737362864:70,361,023C/Tuncertain significance
rs7757414514:70,361,045C/Tuncertain significance
rs10184805444:70,361,060A/Guncertain significance
rs17281228244:70,361,096C/Tuncertain significance
rs3773217774:70,361,142A/Glikely benign
rs1816037904:70,361,182T/Clikely benign
rs7646994594:70,361,249G/Cuncertain significance
rs12078038374:70,361,251G/Auncertain significance
rs7568488574:70,361,264A/Tuncertain significance
rs12250229054:70,361,269G/Cuncertain significance
rs412999784:70,361,342A/Gbenign
rs17281345674:70,361,347G/Tuncertain significance
rs412999764:70,361,348G/Tuncertain significance
rs5341420734:70,361,425T/Cuncertain significance
rs7745664394:70,361,441C/Guncertain significance
rs2005135654:70,361,459T/Auncertain significance
rs412999744:70,361,460C/Gbenign
rs14825622204:70,361,534A/Guncertain significance
rs3701256784:70,361,575G/Auncertain significance
rs131294714:70,362,123G/Aupstream gene variant
rs1509358914:70,373,033T/Cintron variant

Gene information from NCBI Gene. Variant classifications from ClinVar.