RS747813139 CLCN2
Upload your DNA to see your genotype for this variant.
Associated Conditions
Epilepsy
idiopathic generalized
susceptibility to
11
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Familial hyperaldosteronism type II
Epilepsy
idiopathic generalized
susceptibility to
11
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Familial hyperaldosteronism type II
Other Variants in CLCN2