RS201330912 CLCN2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Epilepsy
idiopathic generalized
susceptibility to
11
Familial hyperaldosteronism type II
CLCN2-related disorder
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Epilepsy
idiopathic generalized
susceptibility to
11
Familial hyperaldosteronism type II
CLCN2-related disorder
Other Variants in CLCN2