RS80356690 CLCN1
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What This Variant Does
"rs80356690 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
Myotonia
autosomal recessive form
CLCN1-related disorder
Congenital myotonia
autosomal dominant form
Batten-Turner congenital myopathy
Myotonia
autosomal recessive form
CLCN1-related disorder
Other Variants in CLCN1