RS886041396 ATP1A3
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What This Variant Does
"CLNSIG=5
Associated Conditions
Dystonia 12
Inborn genetic diseases
Developmental and epileptic encephalopathy 99
ATP1A3-related disorder
Dystonia 12
Inborn genetic diseases
Developmental and epileptic encephalopathy 99
ATP1A3-related disorder
Other Variants in ATP1A3