613835.G.1

Country

Palestine

HPO Terms

Visual impairment
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Sex

Unknown

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_201253.3:c.4121_4130del

Remarks

Group consisting of affected members from a large consanguineous Palestinian family
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