RS149316679 CLCN1
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Associated Conditions
Batten-Turner congenital myopathy
Congenital myotonia
autosomal dominant form
autosomal recessive form
Dystonia
early-onset
and/or spastic paraplegia
Batten-Turner congenital myopathy
Congenital myotonia
autosomal dominant form
autosomal recessive form
Dystonia
early-onset
and/or spastic paraplegia
Other Variants in CLCN1