rs146163062

This variant is located in the BICD2 gene.

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ClinVar annotation

Likely Benign★★★☆

2 submitters1 publication

Inborn genetic diseases; Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures

About BICD2

This gene is one of two human homologs of Drosophila bicaudal-D and a member of the Bicoid family. It has been implicated in dynein-mediated, minus end-directed motility along microtubules. It has also been reported to be a phosphorylation target of NIMA related kinase 8. Two alternative splice variants have been described. [provided by RefSeq, Jul 2008]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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