RS80356704 CLCN1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Batten-Turner congenital myopathy
Congenital myotonia
autosomal recessive form
autosomal dominant form
Batten-Turner congenital myopathy
Congenital myotonia
autosomal recessive form
autosomal dominant form
Other Variants in CLCN1