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203780.1
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Subject Details
Country
Lebanon
HPO Terms
Nephrotic syndrome
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Sex
Female
Parental Consanguinity
Yes
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_000092.4:c.1802delC
2
Alport Syndrome 2, Autosomal Recessive
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References
Nair et al. 2018
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