Male
| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_000906.4:c.1768G>A | 2 |
| Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
|---|---|---|---|---|---|---|
| 192600.1.2 | Lebanon | Hypertrophic cardiomyopathy | Male | Sibling of 192600.1.1 |