Gene: VWA3B

Alternate names for this Gene: SCAR22

Gene Summary: This gene encodes an intracellular protein that contains a von Willebrand factor type A domain. Intracellular proteins with VWA domains are thought to function in transcription, DNA repair, ribosomal and membrane transport and the proteasome. Mutations in this gene are associated with Spinocerebellar ataxia, autosomal recessive 22. Alternatively spliced transcript variants have been found for this gene.

Gene is located in Chromosome: 2

Location in Chromosome : 2q11.2

Description of this Gene: von Willebrand factor A domain containing 3B

Type of Gene: protein-coding

rs1394432 in VWA3B gene and Adverse effects, not elsewhere classified PMID 30420678 2019 Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records.