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Date	Panel	Item	Activity
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12 Oct 2020	Intellectual disability - microarray and sequencing v3.421	WNT7A	Arina Puzriakova Source Expert Review Red was added to WNT7A. Rating Changed from Amber List (moderate evidence) to Red List (low evidence)
17 Aug 2020	Intellectual disability - microarray and sequencing v3.255	WNT7A	Arina Puzriakova commented on gene: WNT7A
03 Mar 2020	Intellectual disability - microarray and sequencing v3.3	WNT7A	Zornitza Stark reviewed gene: WNT7A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Fuhrmann syndrome, MIM# 228930, Ulna and fibula, absence of, with severe limb deficiency, MIM# 276820; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
02 Aug 2017	Intellectual disability - microarray and sequencing	WNT7A	BRIDGE consortium edited their review of WNT7A
28 Jul 2017	Intellectual disability - microarray and sequencing	WNT7A	Louise Daugherty classified WNT7A as amber
28 Jul 2017	Intellectual disability - microarray and sequencing	WNT7A	Louise Daugherty commented on WNT7A
27 Jul 2017	Intellectual disability - microarray and sequencing	WNT7A	BRIDGE consortium reviewed WNT7A