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.