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Genomic newborn screening: BabyScreen+ v0.1830 MSH2 Zornitza Stark Classified gene: MSH2 as Green List (high evidence)
Genomic newborn screening: BabyScreen+ v0.1830 MSH2 Zornitza Stark Gene: msh2 has been classified as Green List (High Evidence).
Genomic newborn screening: BabyScreen+ v0.1829 MSH2 Zornitza Stark Tag for review was removed from gene: MSH2.
Genomic newborn screening: BabyScreen+ v0.1829 MSH2 Zornitza Stark edited their review of gene: MSH2: Changed rating: GREEN
Genomic newborn screening: BabyScreen+ v0.1797 MSH2 Zornitza Stark Marked gene: MSH2 as ready
Genomic newborn screening: BabyScreen+ v0.1797 MSH2 Zornitza Stark Gene: msh2 has been classified as Amber List (Moderate Evidence).
Genomic newborn screening: BabyScreen+ v0.1797 MSH2 Zornitza Stark Phenotypes for gene: MSH2 were changed from Lynch syndrome to Mismatch repair cancer syndrome 2, MIM# 619096
Genomic newborn screening: BabyScreen+ v0.1795 MSH2 Zornitza Stark Mode of inheritance for gene: MSH2 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.1794 MSH2 Zornitza Stark Classified gene: MSH2 as Amber List (moderate evidence)
Genomic newborn screening: BabyScreen+ v0.1794 MSH2 Zornitza Stark Gene: msh2 has been classified as Amber List (Moderate Evidence).
Genomic newborn screening: BabyScreen+ v0.1793 MSH2 Zornitza Stark Tag for review tag was added to gene: MSH2.
Tag cancer tag was added to gene: MSH2.
Tag treatable tag was added to gene: MSH2.
Genomic newborn screening: BabyScreen+ v0.1793 MSH2 Zornitza Stark reviewed gene: MSH2: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Mismatch repair cancer syndrome 2, MIM# 619096; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.0 MSH2 Zornitza Stark gene: MSH2 was added
gene: MSH2 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene
Mode of inheritance for gene: MSH2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: MSH2 were set to Lynch syndrome