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Date	Panel	Item	Activity
Filter activities 6 actions
15 Dec 2022	Genomic newborn screening: BabyScreen+ v0.1474	RAB3GAP2	Zornitza Stark Marked gene: RAB3GAP2 as ready
15 Dec 2022	Genomic newborn screening: BabyScreen+ v0.1474	RAB3GAP2	Zornitza Stark Gene: rab3gap2 has been classified as Red List (Low Evidence).
15 Dec 2022	Genomic newborn screening: BabyScreen+ v0.1474	RAB3GAP2	Zornitza Stark Classified gene: RAB3GAP2 as Red List (low evidence)
15 Dec 2022	Genomic newborn screening: BabyScreen+ v0.1474	RAB3GAP2	Zornitza Stark Gene: rab3gap2 has been classified as Red List (Low Evidence).
15 Dec 2022	Genomic newborn screening: BabyScreen+ v0.1473	RAB3GAP2	Zornitza Stark reviewed gene: RAB3GAP2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Warburg micro syndrome 2, MIM# 614225; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Sep 2022	Genomic newborn screening: BabyScreen+ v0.0	RAB3GAP2	Zornitza Stark gene: RAB3GAP2 was added gene: RAB3GAP2 was added to gNBS. Sources: Expert Review Green,BabySeq Category C gene Mode of inheritance for gene: RAB3GAP2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: RAB3GAP2 were set to 20967465; 23420520 Phenotypes for gene: RAB3GAP2 were set to Warburg micro syndrome 2, MIM# 614225