rs104894369(A;G)
From SNPedia
| Familial hypertrophic cardiomyopathy (possible) |
| Is a | genotype |
| of | rs104894369 |
| Gene | MYL2 |
| Chromosome | 12 |
| Position | 110,914,287 |
| Merged from | Rs28933099 |
| mentioned | by |
| Magnitude | 6 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 6 | Familial hypertrophic cardiomyopathy (possible) |
| (G;G) | 0 | common in clinvar |
| (G;T) | 6.2 | Familial Hypertrophic Cardiomyopathy |
see discussion at rs104894369
