RS80356701 CLCN1

Health Risk Chr 7:143330838
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What This Variant Does
"CLNSIG=5
Associated Conditions
Batten-Turner congenital myopathy
Congenital myotonia
autosomal recessive form
autosomal dominant form
CLCN1-related disorder
Batten-Turner congenital myopathy
Congenital myotonia
autosomal recessive form
autosomal dominant form
CLCN1-related disorder
Other Variants in CLCN1
rs121912799 rs80356700 rs1563078827 rs121912801 rs80356694 rs80356696 rs80356690 rs121912805 rs80356702 rs121912807
Ask Dr. Hemsworth about this variant