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613862.4
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Subject Details
Country
Lebanon
HPO Terms
Rod-cone dystrophy
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Sex
Unknown
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_006343.3:c.2079+2T>G
1
Retinitis Pigmentosa 38
NM_006343.3:c.1951C>T
1
Retinitis Pigmentosa 38
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References
Audo et al. 2018
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