RS1563073737 CLCN1

Health Risk Chr 7:143320673
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Associated Conditions
Inborn genetic diseases
Congenital myotonia
autosomal recessive form
autosomal dominant form
Inborn genetic diseases
Congenital myotonia
autosomal recessive form
autosomal dominant form
Other Variants in CLCN1
rs121912799 rs80356700 rs1563078827 rs121912801 rs80356694 rs80356696 rs80356690 rs121912805 rs80356702 rs121912807
Ask Dr. Hemsworth about this variant