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Date	Panel	Item	Activity
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09 Nov 2021	Fetal anomalies v0.342	BRIP1	Zornitza Stark changed review comment from: Well established gene-disease association.; to: Well established gene-disease association, multiple congenital anomaly syndrome.
09 Nov 2021	Fetal anomalies v0.342	BRIP1	Zornitza Stark Marked gene: BRIP1 as ready
09 Nov 2021	Fetal anomalies v0.342	BRIP1	Zornitza Stark Gene: brip1 has been classified as Green List (High Evidence).
09 Nov 2021	Fetal anomalies v0.342	BRIP1	Zornitza Stark Phenotypes for gene: BRIP1 were changed from FANCONI ANEMIA, COMPLEMENTATION GROUP J to Fanconi anemia, complementation group J, MIM# 609054
24 Oct 2021	Fetal anomalies v0.0	BRIP1	Zornitza Stark gene: BRIP1 was added gene: BRIP1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp Mode of inheritance for gene: BRIP1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: BRIP1 were set to FANCONI ANEMIA, COMPLEMENTATION GROUP J