RS80356699 CLCN1
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What This Variant Does
"rs80356699 is a mutation in the CLCN1 gene on chromosome 7. Acting in an autosomal dominant manner, ...
Associated Conditions
Congenital myotonia
autosomal dominant form
Batten-Turner congenital myopathy
autosomal recessive form
Congenital myotonia
autosomal dominant form
Batten-Turner congenital myopathy
autosomal recessive form
Other Variants in CLCN1