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17 Jun 2019	Haematuria v1.28	NPHS2	Eleanor Williams Phenotypes for gene: NPHS2 were changed from Hematuria, Benign Familial; Alport Syndrome, X-Linked; Alport Syndrome, Autosomal Recessive; Alport Syndrome, Autosomal Dominant; Nephrotic Syndrome, Type 2 to Hematuria, Benign Familial; Alport Syndrome, X-Linked; Alport Syndrome, Autosomal Recessive; Alport Syndrome, Autosomal Dominant; Nephrotic Syndrome, Type 2; ?Modifier of COL4A variants
17 Jun 2019	Haematuria v1.27	NPHS2	Eleanor Williams Publications for gene: NPHS2 were set to
06 Feb 2019	Haematuria v1.18	NPHS2	Anna de Burca reviewed gene: NPHS2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
03 Feb 2019	Haematuria v1.18	NPHS2	Eleanor Williams reviewed gene: NPHS2: Rating: AMBER; Mode of pathogenicity: ; Publications: PMID: 26138234; Phenotypes: ?Modifier of COL4A variants; Mode of inheritance: Unknown; Current diagnostic: yes
03 Feb 2019	Haematuria v1.17	NPHS2	Eleanor Williams Source NHS GMS was added to NPHS2.