rs104894729(G;G)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs104894729 |
| Gene | TNNI3 |
| Chromosome | 19 |
| Position | 55,151,892 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 6 | Familial restrictive cardiomyopathy, type 1 |
| (A;G) | 6.2 | Familial Hypertrophic Cardiomyopathy |
| (C;G) | 6.2 | Familial Hypertrophic Cardiomyopathy |
| (G;G) | 0 | common in clinvar |
| (G;T) | 6.2 | Familial Hypertrophic Cardiomyopathy |
