rs111377893(C;C)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs111377893 |
| Gene | TNNT2 |
| Chromosome | 1 |
| Position | 201,359,622 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (A;C) | 6.2 | Familial Hypertrophic Cardiomyopathy |
| (C;C) | 0 | common in clinvar |
| (C;G) | 6.2 | Familial Hypertrophic Cardiomyopathy |
| (C;T) | 6.2 | Familial Hypertrophic Cardiomyopathy |
