rs80356690(C;C)

common in clinvar

Is a	genotype
of	rs80356690
Gene	CLCN1
Chromosome	7
Position	143,330,788
Merged from	Rs121912804
mentioned	by

Magnitude

0

Repute

Good

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