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535000.2
Home
Subject Details
Country
Lebanon
HPO Terms
Visual impairment
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Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NC_012920.1:m.14568C>T
Leber Optic Atrophy
NC_012920.1:m.7299A>G
Leber Optic Atrophy
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References
Rizk et al. 2020
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