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Date	Panel	Item	Activity
Filter activities 10 actions
28 Jul 2024	BabyScreen+ newborn screening v1.114	SLC12A3	Tommy Li Added phenotypes Gitelman syndrome, MIM# 263800 for gene: SLC12A3
09 Nov 2022	BabyScreen+ newborn screening v0.866	SLC12A3	Zornitza Stark Tag for review was removed from gene: SLC12A3.
31 Oct 2022	BabyScreen+ newborn screening v0.713	SLC12A3	Seb Lunke Marked gene: SLC12A3 as ready
31 Oct 2022	BabyScreen+ newborn screening v0.713	SLC12A3	Seb Lunke Gene: slc12a3 has been classified as Red List (Low Evidence).
31 Oct 2022	BabyScreen+ newborn screening v0.713	SLC12A3	Seb Lunke Phenotypes for gene: SLC12A3 were changed from Gitelman syndrome to Gitelman syndrome, MIM# 263800
31 Oct 2022	BabyScreen+ newborn screening v0.712	SLC12A3	Seb Lunke Classified gene: SLC12A3 as Red List (low evidence)
31 Oct 2022	BabyScreen+ newborn screening v0.712	SLC12A3	Seb Lunke Gene: slc12a3 has been classified as Red List (Low Evidence).
31 Oct 2022	BabyScreen+ newborn screening v0.711	SLC12A3	Seb Lunke Tag for review tag was added to gene: SLC12A3.
31 Oct 2022	BabyScreen+ newborn screening v0.711	SLC12A3	Seb Lunke reviewed gene: SLC12A3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Gitelman syndrome, MIM# 263800; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Sep 2022	BabyScreen+ newborn screening v0.0	SLC12A3	Zornitza Stark gene: SLC12A3 was added gene: SLC12A3 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green Mode of inheritance for gene: SLC12A3 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SLC12A3 were set to Gitelman syndrome