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Optic neuropathy v1.79 | RAB3GAP1 | Ivone Leong Phenotypes for gene: RAB3GAP1 were changed from to WARBURG MICRO SYNDROME 1, 600118 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Optic neuropathy v1.78 | RAB3GAP1 | Ivone Leong Publications for gene: RAB3GAP1 were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Optic neuropathy v1.77 | RAB3GAP1 | Ivone Leong Mode of inheritance for gene: RAB3GAP1 was changed from to BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Optic neuropathy v1.28 | RAB3GAP1 | Tom Cullup reviewed gene: RAB3GAP1: Rating: RED; Mode of pathogenicity: ; Publications: 26421802; Phenotypes: WARBURG MICRO SYNDROME 1, 600118; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Optic neuropathy v1.27 | RAB3GAP1 |
Ivone Leong gene: RAB3GAP1 was added gene: RAB3GAP1 was added to Optic neuropathy. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: RAB3GAP1 was set to |