RS776173406 CLCN1
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Associated Conditions
Congenital myotonia
autosomal dominant form
autosomal recessive form
Congenital myotonia
autosomal dominant form
autosomal recessive form
CLCN1-related disorder
Congenital myotonia
autosomal dominant form
autosomal recessive form
Congenital myotonia
autosomal dominant form
autosomal recessive form
CLCN1-related disorder
Other Variants in CLCN1