604116.G.1

Country

Syria

HPO Terms

Visual impairment; Cone/cone-rod dystrophy
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Sex

Unknown

Family History

Yes

Parental Consanguinity

No

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_000350.3:c.3610G>A4

Remarks

2 members of a family
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