rs80356686(A;G)

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

Is a	genotype
of	rs80356686
Gene	CLCN1
Chromosome	7
Position	143,321,729
mentioned	by

Magnitude

4

Repute

Bad

Geno	Mag	Summary
(A;G)	4	Myotonia congenita; Thomsen's disease; quite variable in degree
(G;G)	0	common in clinvar