rs121917761(A;A)
From SNPedia
| Familial restrictive cardiomyopathy, type 1, as a possibility |
| Is a | genotype |
| of | rs121917761 |
| Gene | TNNI3 |
| Chromosome | 19 |
| Position | 55,154,068 |
| mentioned | by |
| Magnitude | 5 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 5 | Familial restrictive cardiomyopathy, type 1, as a possibility |
| (A;G) | 5 | Familial restrictive cardiomyopathy, type 1 as a possibility |
| (G;G) | 0 | common in clinvar |
See discussion at rs121917761.
