rs2493174263
This variant is located in the CWF19L1 gene.
▶ClinVar annotation
About CWF19L1
This gene encodes a member of the CWF19 protein family. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia-17 and mild cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
View all CWF19L1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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