RS1057518917 FAM131B;CLCN1

Health Risk Chr 7:143351633

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What This Variant Does

"CLNSIG=5

Associated Conditions

Myotonia

Congenital myotonia

autosomal recessive form

autosomal dominant form

Myotonia

Congenital myotonia

autosomal recessive form

autosomal dominant form

Ask Dr. Hemsworth about this variant