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BabyScreen+ newborn screening v1.114 SLC6A5 Tommy Li Added phenotypes Hyperekplexia 3, MIM#614618 for gene: SLC6A5
BabyScreen+ newborn screening v0.1355 SLC6A5 Seb Lunke Marked gene: SLC6A5 as ready
BabyScreen+ newborn screening v0.1355 SLC6A5 Seb Lunke Gene: slc6a5 has been classified as Amber List (Moderate Evidence).
BabyScreen+ newborn screening v0.1355 SLC6A5 Seb Lunke Classified gene: SLC6A5 as Amber List (moderate evidence)
BabyScreen+ newborn screening v0.1355 SLC6A5 Seb Lunke Gene: slc6a5 has been classified as Amber List (Moderate Evidence).
BabyScreen+ newborn screening v0.1354 SLC6A5 Seb Lunke Tag for review tag was added to gene: SLC6A5.
BabyScreen+ newborn screening v0.1354 SLC6A5 Seb Lunke reviewed gene: SLC6A5: Rating: AMBER; Mode of pathogenicity: None; Publications: 20301437; Phenotypes: Hyperekplexia 3, MIM# 614618; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 SLC6A5 Zornitza Stark gene: SLC6A5 was added
gene: SLC6A5 was added to gNBS. Sources: BeginNGS,BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: SLC6A5 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: SLC6A5 were set to Hyperekplexia 3, MIM#614618