Male
| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_001363711.1:c.3082_3085delinsGCTTCCT | 1 |
| Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
|---|---|---|---|---|---|---|
| 607200.1.1 | Oman | Congenital hypothyroidism | Male | Yes | ||
| 607200.1.2 | Oman | Male |