rs28932774(C;T)
From SNPedia
| Familial Hypertrophic Cardiomyopathy |
| Is a | genotype |
| of | rs28932774 |
| Gene | MYL2 |
| Chromosome | 12 |
| Position | 110,919,145 |
| Merged into | Rs104894370 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 3 | Familial Hypertrophic Cardiomyopathy |
| (C;T) | 3 | Familial Hypertrophic Cardiomyopathy |
| (T;T) | 0 |
Familial hypertrophic cardiomyopathy
see also OMIM 160781.0005
