613428.1

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Country

Lebanon

HPO Terms

Optic atrophy; Chorioretinal atrophy; Retinopathy
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Sex

Male

Parental Consanguinity

No

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001029883.3:c.2756_2758del1
NM_001029883.3:c.802C>T1
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Remarks

Lebanese/Armenian origin

References

© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.