RS71318369 CLCN2
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What This Variant Does
"[OMIM:?]
Associated Conditions
EPILEPSY
JUVENILE MYOCLONIC
SUSCEPTIBILITY TO
8
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Epilepsy
idiopathic generalized
susceptibility to
11
Familial hyperaldosteronism type II
EPILEPSY
JUVENILE MYOCLONIC
SUSCEPTIBILITY TO
8
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Other Variants in CLCN2