rs104894724(C;C)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs104894724 |
| Gene | TNNI3 |
| Chromosome | 19 |
| Position | 55,154,146 |
| Merged from | Rs28934871 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;G) | 6.2 | Familial Hypertrophic Cardiomyopathy |
| (C;T) | 6.2 | Familial Hypertrophic Cardiomyopathy |
| (G;G) | 5 | Familial hypertrophic cardiomyopathy, type 7 |
| (T;T) | 5 | Familial restrictive cardiomyopathy, type 1 |
