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Date	Panel	Item	Activity
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19 Jun 2019	Structural eye disease v0.76	SLC24A1	Nicola Ragge reviewed gene: SLC24A1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Night blindness, congenital stationary (complete), 1D, autosomal recessive, 613830; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Apr 2019	Structural eye disease v0.48	SLC24A1	Ivone Leong edited their review of gene: SLC24A1: Changed phenotypes: Night blindness, congenital stationary (complete), 1D, autosomal recessive, 613830
17 Apr 2019	Structural eye disease v0.38	SLC24A1	Ivone Leong reviewed gene: SLC24A1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ALBINISM, OCULOCUTANEOUS, TYPE VI, 113750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
17 Apr 2019	Structural eye disease v0.15	SLC24A1	Ivone Leong Source NHS GMS was added to SLC24A1. Mode of inheritance for gene SLC24A1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Night blindness, congenital stationary (complete), 1D, autosomal recessive, 613830 for gene: SLC24A1
03 Jan 2019	Structural eye disease v0.2	SLC24A1	Ellen McDonagh gene: SLC24A1 was added gene: SLC24A1 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: SLC24A1 was set to Phenotypes for gene: SLC24A1 were set to Eye Disorders