rs80356689(C;T)

Myotonia congenita; Thomsen's disease; quite variable in degree

Is a	genotype
of	rs80356689
Gene	CLCN1
Chromosome	7
Position	143,330,775
mentioned	by

Magnitude

4

Repute

Bad

Geno	Mag	Summary
(C;T)	4	Myotonia congenita; Thomsen's disease; quite variable in degree
(T;T)	0	common in clinvar