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Date	Panel	Item	Activity
Filter activities 7 actions
28 Jan 2022	Fetal anomalies v0.2918	SNRPE	Zornitza Stark Marked gene: SNRPE as ready
28 Jan 2022	Fetal anomalies v0.2918	SNRPE	Zornitza Stark Gene: snrpe has been classified as Red List (Low Evidence).
28 Jan 2022	Fetal anomalies v0.2918	SNRPE	Zornitza Stark Phenotypes for gene: SNRPE were changed from AUTOSOMAL-DOMINANT HYPOTRICHOSIS SIMPLEX to Hypotrichosis 11, MIM #615059
28 Jan 2022	Fetal anomalies v0.2917	SNRPE	Zornitza Stark Mode of inheritance for gene: SNRPE was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
28 Jan 2022	Fetal anomalies v0.2916	SNRPE	Zornitza Stark Classified gene: SNRPE as Red List (low evidence)
28 Jan 2022	Fetal anomalies v0.2916	SNRPE	Zornitza Stark Gene: snrpe has been classified as Red List (Low Evidence).
24 Oct 2021	Fetal anomalies v0.0	SNRPE	Zornitza Stark gene: SNRPE was added gene: SNRPE was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: SNRPE was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: SNRPE were set to AUTOSOMAL-DOMINANT HYPOTRICHOSIS SIMPLEX