RS121912805 CLCN1

Health Risk Chr 7:143330789
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What This Variant Does
"rs121912805, also known as c.871G&gt
Associated Conditions
Congenital myotonia
autosomal recessive form
autosomal dominant form
Congenital myotonia
autosomal recessive form
Congenital myotonia
autosomal recessive form
autosomal dominant form
Congenital myotonia
autosomal recessive form
Other Variants in CLCN1
rs121912799 rs80356700 rs1563078827 rs121912801 rs80356694 rs80356696 rs80356690 rs80356702 rs121912807 rs140026363
Ask Dr. Hemsworth about this variant