rs778157390
This variant is located in the ZNF592 gene.
▶ClinVar annotation
About ZNF592
This gene is thought to play a role in a complex developmental pathway and the regulation of genes involved in cerebellar development. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia. [provided by RefSeq, Jan 2011]
View all ZNF592 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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