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| Groopman et al 2019 - Genes with diagnostic variants v0.4 | KLHL3 | Eleanor Williams reviewed gene: KLHL3: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Groopman et al 2019 - Genes with diagnostic variants v0.3 | KLHL3 | Eleanor Williams Source Expert Review Red was added to KLHL3. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Groopman et al 2019 - Genes with diagnostic variants v0.2 | KLHL3 |
Eleanor Williams gene: KLHL3 was added gene: KLHL3 was added to Groopman et al 2019 - Genes with diagnostic variants. Sources: Literature,Expert review red Mode of inheritance for gene: KLHL3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: KLHL3 were set to Other; MIM 614495; Pseudohypoaldosteronism type IID |
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