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Date	Panel	Item	Activity
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12 Oct 2020	Intellectual disability - microarray and sequencing v3.421	SCN4A	Arina Puzriakova Source Expert Review Red was added to SCN4A. Rating Changed from Amber List (moderate evidence) to Red List (low evidence)
17 Aug 2020	Intellectual disability - microarray and sequencing v3.254	SCN4A	Arina Puzriakova commented on gene: SCN4A
07 Feb 2020	Intellectual disability - microarray and sequencing v3.0	SCN4A	Zornitza Stark reviewed gene: SCN4A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hyperkalemic periodic paralysis, type 2, MIM# 170500, Hypokalemic periodic paralysis, type 2, MIM# 613345, Myasthenic syndrome, congenital, 16, MIM# 614198, Myotonia congenita, atypical, acetazolamide-responsive 608390, Paramyotonia congenita 168300; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
30 Jan 2020	Intellectual disability - microarray and sequencing v3.0	SCN4A	Andrea Haworth commented on gene: SCN4A
02 Aug 2017	Intellectual disability - microarray and sequencing	SCN4A	BRIDGE consortium edited their review of SCN4A
27 Jul 2017	Intellectual disability - microarray and sequencing	SCN4A	BRIDGE consortium edited their review of SCN4A
20 Jul 2017	Intellectual disability - microarray and sequencing	SCN4A	Louise Daugherty classified SCN4A as amber
20 Jul 2017	Intellectual disability - microarray and sequencing	SCN4A	Louise Daugherty commented on SCN4A
19 Jul 2017	Intellectual disability - microarray and sequencing	SCN4A	BRIDGE consortium reviewed SCN4A