Male
No
Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
---|---|---|---|---|
NM_001206744.2:c.1472G>A | 2 | |||
NM_003235.5:c.4930C>G | 1 |
Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
---|---|---|---|---|---|---|
274500.1 | United Arab Emirates | Congenital hypothyroidism | No | Yes |