615761.1

Country

United Arab Emirates

HPO Terms

Global developmental delay; Hypoglycemia; Polydactyly
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Sex

Female

Family History

No

Parental Consanguinity

No

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001080517.2:c.2347-7A>G1

Remarks

de novo mutation
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