rs80356695(C;C)

common in clinvar

Is a	genotype
of	rs80356695
Gene	CLCN1
Chromosome	7
Position	143,339,289
mentioned	by

Magnitude

0

Repute

Good

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