Unknown
| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_001089.2:c.446C>T | 1 | |||
| NM_001369.2:c.5503C>T | 1 |
| Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
|---|---|---|---|---|---|---|
| 610921.3 | United Arab Emirates | Unknown | Article does not list phenotype. Patient remark from article: "Individual screened for genetic disorders". |