rs80356696(A;A)

common in clinvar

Is a	genotype
of	rs80356696
Gene	CLCN1
Chromosome	7
Position	143,342,001
Merged from	Rs121912803
mentioned	by

Magnitude

0

Repute

Good

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