rs80356696(A;G)
From SNPedia
| Myotonia congenita; Thomsen's disease; quite variable in degree |
| Is a | genotype |
| of | rs80356696 |
| Gene | CLCN1 |
| Chromosome | 7 |
| Position | 143,342,001 |
| Merged from | Rs121912803 |
| 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
