RS1085307989 CLCN1

Health Risk Chr 7:143331583
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What This Variant Does
"CLNSIG=4
Associated Conditions
Congenital myotonia
autosomal dominant form
autosomal recessive form
Congenital myotonia
autosomal dominant form
autosomal recessive form
Other Variants in CLCN1
rs121912799 rs80356700 rs1563078827 rs121912801 rs80356694 rs80356696 rs80356690 rs121912805 rs80356702 rs121912807
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