RS764793623 CLCN2

Health Risk Chr 3:184357011
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Associated Conditions
Inborn genetic diseases
Epilepsy
idiopathic generalized
susceptibility to
11
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Familial hyperaldosteronism type II
Inborn genetic diseases
Epilepsy
idiopathic generalized
susceptibility to
11
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Familial hyperaldosteronism type II
Other Variants in CLCN2
rs515726131 rs71318369 rs137852682 rs201330912 rs587777110 rs587777111 rs587777112 rs376823689 rs371193424 rs141242566
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