rs104894730(G;G)
From SNPedia
| Familial restrictive cardiomyopathy, type 1 |
| Is a | genotype |
| of | rs104894730 |
| Gene | TNNI3 |
| Chromosome | 19 |
| Position | 55,154,047 |
| Merged from | Rs28934870 |
| mentioned | by |
| Magnitude | 6 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (A;G) | 5 | Familial restrictive cardiomyopathy, type 1 |
| (G;G) | 6 | Familial restrictive cardiomyopathy, type 1 |
See discussion at rs104894730
