rs80356694(C;T)

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

Is a	genotype
of	rs80356694
Gene	CLCN1
Chromosome	7
Position	143,339,290
Merged from	Rs121912802
mentioned	by

Magnitude

4

Repute

Bad

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