rs80356699(A;G)
From SNPedia
Myotonia congenita; Thomsen's disease; quite variable in degree |
Is a | genotype |
of | rs80356699 |
Gene | CLCN1 |
Chromosome | 7 |
Position | 143,320,744 |
Merged from | Rs121912809 |
mentioned | by |
Magnitude | 4 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
(A;G) | 4 | Myotonia congenita; Thomsen's disease; quite variable in degree |
See discussion at myotonia congenita