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| DDG2P v3.12 | CD96 | Achchuthan Shanmugasundram reviewed gene: CD96: Rating: RED; Mode of pathogenicity: ; Publications: 17847009; Phenotypes: C SYNDROME, OMIM:211750; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| DDG2P v3.11 | CD96 |
Achchuthan Shanmugasundram Source Expert Review Red was added to CD96. Rating Changed from Amber List (moderate evidence) to Red List (low evidence) |
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| DDG2P v0.2 | CD96 | Rebecca Foulger reviewed gene: CD96: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| DDG2P v0.1 | CD96 |
Rebecca Foulger gene: CD96 was added gene: CD96 was added to DDG2P. Sources: Expert Review Amber,DD-Gene2Phenotype Mode of inheritance for gene: CD96 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: CD96 were set to 17847009 Phenotypes for gene: CD96 were set to C SYNDROME 211750 |
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