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Date	Panel	Item	Activity
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12 Oct 2020	Intellectual disability - microarray and sequencing v3.421	LTBP2	Arina Puzriakova Source Expert Review Red was added to LTBP2. Rating Changed from Amber List (moderate evidence) to Red List (low evidence)
17 Aug 2020	Intellectual disability - microarray and sequencing v3.253	LTBP2	Arina Puzriakova commented on gene: LTBP2
09 Feb 2020	Intellectual disability - microarray and sequencing v3.0	LTBP2	Zornitza Stark reviewed gene: LTBP2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Weill-Marchesani syndrome 3, recessive, MIM# 614819, Glaucoma 3, primary congenital, MIM# 613086, Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma, MIM# 251750; Mode of inheritance: None
02 Aug 2017	Intellectual disability - microarray and sequencing	LTBP2	BRIDGE consortium edited their review of LTBP2
28 Jul 2017	Intellectual disability - microarray and sequencing	LTBP2	Louise Daugherty classified LTBP2 as amber
28 Jul 2017	Intellectual disability - microarray and sequencing	LTBP2	Louise Daugherty commented on LTBP2
27 Jul 2017	Intellectual disability - microarray and sequencing	LTBP2	BRIDGE consortium reviewed LTBP2