RS782583311 ATP1A3
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Associated Conditions
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
Dystonia 12
Inborn genetic diseases
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
Dystonia 12
Inborn genetic diseases
Other Variants in ATP1A3