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Genomic newborn screening: BabyScreen+ v1.136 MYL2 Zornitza Stark Marked gene: MYL2 as ready
Genomic newborn screening: BabyScreen+ v1.136 MYL2 Zornitza Stark Gene: myl2 has been classified as Amber List (Moderate Evidence).
Genomic newborn screening: BabyScreen+ v1.136 MYL2 Zornitza Stark Phenotypes for gene: MYL2 were changed from Cardiomyopathy, familial hypertrophic, 10 to Cardiomyopathy, hypertrophic, 10, MIM# 608758
Genomic newborn screening: BabyScreen+ v1.135 MYL2 Zornitza Stark reviewed gene: MYL2: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Cardiomyopathy, hypertrophic, 10, MIM# 608758; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Genomic newborn screening: BabyScreen+ v0.0 MYL2 Zornitza Stark gene: MYL2 was added
gene: MYL2 was added to gNBS. Sources: Expert Review Amber,BabySeq Category B gene
Mode of inheritance for gene: MYL2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: MYL2 were set to Cardiomyopathy, familial hypertrophic, 10