Activity
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2 actions
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| Additional findings_Paediatric v0.2 | KCNE1 |
Zornitza Stark Source BabySeq Category B gene was added to KCNE1. Source Expert Review Amber was added to KCNE1. Mode of inheritance for gene KCNE1 was changed from BIALLELIC, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Long QT syndrome-5 for gene: KCNE1 Rating Changed from Green List (high evidence) to Amber List (moderate evidence) |
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| Additional findings_Paediatric v0.2 | KCNE1 |
Zornitza Stark gene: KCNE1 was added gene: KCNE1 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene Mode of inheritance for gene: KCNE1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: KCNE1 were set to Jervell and Lange-Nielsen syndrome |
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