rs80356699(A;A)

common in clinvar

Is a	genotype
of	rs80356699
Gene	CLCN1
Chromosome	7
Position	143,320,744
Merged from	Rs121912809
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