rs104894845(A;G)
From SNPedia
| Familial hypertrophic cardiomyopathy possible; but significance is uncertain |
| Is a | genotype |
| of | rs104894845 |
| Gene | GLA, RPL36A-HNRNPH2 |
| Chromosome | X |
| Position | 101,401,752 |
| mentioned | by |
| Magnitude | 4 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 4 | Familial hypertrophic cardiomyopathy possible; but significance is uncertain |
| (G;G) | 0 | common in clinvar |
see discussion at rs104894845
