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Groopman et al 2019 - Genes with diagnostic variants v0.4 | CRB2 | Eleanor Williams reviewed gene: CRB2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Groopman et al 2019 - Genes with diagnostic variants v0.3 | CRB2 |
Eleanor Williams Source Expert Review Amber was added to CRB2. Rating Changed from Red List (low evidence) to Amber List (moderate evidence) |
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Groopman et al 2019 - Genes with diagnostic variants v0.2 | CRB2 |
Eleanor Williams gene: CRB2 was added gene: CRB2 was added to Groopman et al 2019 - Genes with diagnostic variants. Sources: Literature,Exper review amber Mode of inheritance for gene: CRB2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: CRB2 were set to Focal segmental glomerulosclerosis 9; Glomerulopathy; MIM 616220 |