RS782175860 ATP1A3

Health Risk Chr 19:41975776
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What This Variant Does
"CLNSIG=5
Associated Conditions
Alternating hemiplegia of childhood 2
Dystonia 12
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
Developmental and epileptic encephalopathy 99
Dystonia 12
Seizure
Inborn genetic diseases
Alternating hemiplegia of childhood 2
Dystonia 12
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
Developmental and epileptic encephalopathy 99
Dystonia 12
Seizure
Inborn genetic diseases
Other Variants in ATP1A3
rs80356534 rs80356532 rs80356533 rs80356535 rs80356536 rs80356537 rs267606670 rs387907281 rs387907282 rs398122887
Ask Dr. Hemsworth about this variant