RS377119457 CLCN2
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Associated Conditions
Familial hyperaldosteronism type II
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Epilepsy
idiopathic generalized
susceptibility to
11
Hereditary ataxia
Familial hyperaldosteronism type II
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Epilepsy
idiopathic generalized
susceptibility to
11
Hereditary ataxia
Other Variants in CLCN2