RS80356696 CLCN1

Health Risk Chr 7:143342001
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What This Variant Does
"rs80356696, also known as c.1655A&gt
Associated Conditions
Myotonia levior
Batten-Turner congenital myopathy
Congenital myotonia
autosomal recessive form
autosomal dominant form
Myotonia levior
Batten-Turner congenital myopathy
Congenital myotonia
autosomal recessive form
autosomal dominant form
Other Variants in CLCN1
rs121912799 rs80356700 rs1563078827 rs121912801 rs80356694 rs80356690 rs121912805 rs80356702 rs121912807 rs140026363
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