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Date	Panel	Item	Activity
Filter activities 7 actions
23 Sep 2022	Genomic newborn screening: BabyScreen+ v0.152	BBS7	Zornitza Stark Marked gene: BBS7 as ready
23 Sep 2022	Genomic newborn screening: BabyScreen+ v0.152	BBS7	Zornitza Stark Gene: bbs7 has been classified as Red List (Low Evidence).
23 Sep 2022	Genomic newborn screening: BabyScreen+ v0.152	BBS7	Zornitza Stark Phenotypes for gene: BBS7 were changed from Bardet-Biedl syndrome to Bardet-Biedl syndrome 7, MIM# 615984
23 Sep 2022	Genomic newborn screening: BabyScreen+ v0.151	BBS7	Zornitza Stark Classified gene: BBS7 as Red List (low evidence)
23 Sep 2022	Genomic newborn screening: BabyScreen+ v0.151	BBS7	Zornitza Stark Gene: bbs7 has been classified as Red List (Low Evidence).
23 Sep 2022	Genomic newborn screening: BabyScreen+ v0.150	BBS7	Zornitza Stark reviewed gene: BBS7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Bardet-Biedl syndrome 7, MIM# 615984; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Sep 2022	Genomic newborn screening: BabyScreen+ v0.0	BBS7	Zornitza Stark gene: BBS7 was added gene: BBS7 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green Mode of inheritance for gene: BBS7 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: BBS7 were set to Bardet-Biedl syndrome