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Groopman et al 2019 - Genes with diagnostic variants v0.4 | NPHS2 | Eleanor Williams reviewed gene: NPHS2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Groopman et al 2019 - Genes with diagnostic variants v0.3 | NPHS2 |
Eleanor Williams Source Expert Review Green was added to NPHS2. Rating Changed from Red List (low evidence) to Green List (high evidence) |
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Groopman et al 2019 - Genes with diagnostic variants v0.2 | NPHS2 |
Eleanor Williams gene: NPHS2 was added gene: NPHS2 was added to Groopman et al 2019 - Genes with diagnostic variants. Sources: Literature,Expert review green Mode of inheritance for gene: NPHS2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: NPHS2 were set to Nephropathy of unknown origin; Hypertensive nephropathy; Glomerulopathy; Nephrotic syndrome type 2; MIM 600995 |