RS606231435 ATP1A3
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Dystonia 12
Alternating hemiplegia of childhood 2
Inborn genetic diseases
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
ATP1A3-associated neurological disorder
ATP1A3-related disorder
Dystonia 12
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
Dystonia 12
Alternating hemiplegia of childhood 2
Inborn genetic diseases
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
ATP1A3-associated neurological disorder
ATP1A3-related disorder
Dystonia 12
Other Variants in ATP1A3