rs45496496(C;G)
From SNPedia
| Variant of unclear significance |
| Is a | genotype |
| of | rs45496496 |
| Gene | MYH7 |
| Chromosome | 14 |
| Position | 23,423,939 |
| mentioned | by |
| Magnitude | 3 |
| Geno | Mag | Summary |
|---|---|---|
| (C;G) | 3 | Variant of unclear significance |
| (G;G) | 0 | common in clinvar |
Very rare variant; significance unclear. See discussion at rs45496496
