Condition: Vertigo


rs151344517 in LOC107985154;AFG3L2;TUBB6 gene and Vertigo PMID 20725928 2010 Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias.

rs796053124 in SCN2A gene and Vertigo PMID 20956790 2010 SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain.