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600995.3
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Subject Details
Country
Lebanon
HPO Terms
Nephrotic syndrome; Global developmental delay
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Sex
Unknown
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_014625.4:c.538G>A
1
Nephrotic Syndrome, Type 2
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References
Jalkh et al. 2019
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