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BabyScreen+ newborn screening v0.1411 SNAP25 Seb Lunke Marked gene: SNAP25 as ready
BabyScreen+ newborn screening v0.1411 SNAP25 Seb Lunke Gene: snap25 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.1411 SNAP25 Seb Lunke Tag for review tag was added to gene: SNAP25.
BabyScreen+ newborn screening v0.1411 SNAP25 Seb Lunke Phenotypes for gene: SNAP25 were changed from Myasthenic syndrome, congenital, 18, MIM# 616330 to Neurodevelopmental disorder, MONDO:0700092, SNAP25-related
BabyScreen+ newborn screening v0.1410 SNAP25 Seb Lunke Publications for gene: SNAP25 were set to
BabyScreen+ newborn screening v0.1409 SNAP25 Seb Lunke Classified gene: SNAP25 as Red List (low evidence)
BabyScreen+ newborn screening v0.1409 SNAP25 Seb Lunke Gene: snap25 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.1408 SNAP25 Seb Lunke reviewed gene: SNAP25: Rating: RED; Mode of pathogenicity: None; Publications: 20301347; Phenotypes: Neurodevelopmental disorder, MONDO:0700092, SNAP25-related; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
BabyScreen+ newborn screening v0.0 SNAP25 Zornitza Stark gene: SNAP25 was added
gene: SNAP25 was added to gNBS. Sources: BeginNGS,Expert Review Green
Mode of inheritance for gene: SNAP25 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: SNAP25 were set to Myasthenic syndrome, congenital, 18, MIM# 616330