APOL4

apolipoprotein L4

Summary

This gene encodes a member of the apolipoprotein L family. The encoded protein may play a role in lipid exchange and transport throughout the body, as well as in reverse cholesterol transport from peripheral cells to the liver. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2020]

Known Variants7 total

rsidPosition (GRCh37)AllelesClassClinVar
rs75855186322:36,587,938T/Cuncertain significance
rs74787101122:36,591,441T/Auncertain significance
rs77473858522:36,591,474C/Tuncertain significance
rs251783703822:36,595,377T/Glikely benign
rs20097857722:36,595,387C/Tuncertain significance
rs20135575022:36,595,421C/Tlikely benign
rs75827006522:36,598,042A/Tuncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.