rs397516463(C;T)
From SNPedia
| Familial hypertrophic cardiomyopathy (possible) |
| Is a | genotype |
| of | rs397516463 |
| Gene | TNNT2 |
| Chromosome | 1 |
| Position | 201,364,369 |
| mentioned | by |
| Magnitude | 6 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 6 | Familial hypertrophic cardiomyopathy (possible) |
see discussion at rs397516463
