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Date	Panel	Item	Activity
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01 Mar 2022	Intellectual disability - microarray and sequencing v3.1504	KCNE1	Arina Puzriakova Mode of inheritance for gene: KCNE1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
01 Mar 2022	Intellectual disability - microarray and sequencing v3.1503	KCNE1	Arina Puzriakova Phenotypes for gene: KCNE1 were changed from NA to Jervell and Lange-Nielsen syndrome 2, OMIM:612347; Long QT syndrome 5, OMIM:613695
11 Feb 2021	Intellectual disability - microarray and sequencing v3.890	KCNE1	Sarah Leigh Source: Expert Review Amber was removed from gene: KCNE1
02 Aug 2017	Intellectual disability - microarray and sequencing	KCNE1	BRIDGE consortium edited their review of KCNE1
28 Jul 2017	Intellectual disability - microarray and sequencing	KCNE1	Louise Daugherty classified KCNE1 as amber
28 Jul 2017	Intellectual disability - microarray and sequencing	KCNE1	Louise Daugherty commented on KCNE1
27 Jul 2017	Intellectual disability - microarray and sequencing	KCNE1	BRIDGE consortium reviewed KCNE1