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Groopman et al 2019 - Genes with diagnostic variants v0.4 | SLC34A3 | Eleanor Williams reviewed gene: SLC34A3: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Groopman et al 2019 - Genes with diagnostic variants v0.3 | SLC34A3 | Eleanor Williams Source Expert Review Red was added to SLC34A3. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Groopman et al 2019 - Genes with diagnostic variants v0.2 | SLC34A3 |
Eleanor Williams gene: SLC34A3 was added gene: SLC34A3 was added to Groopman et al 2019 - Genes with diagnostic variants. Sources: Literature,Expert review red Mode of inheritance for gene: SLC34A3 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SLC34A3 were set to MIM 241530; Nephropathy of unknown origin; Hypophosphatemic rickets with hypercalciuria |