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Date	Panel	Item	Activity
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13 Jan 2022	Fetal anomalies v0.1972	NSD2	Zornitza Stark Marked gene: NSD2 as ready
13 Jan 2022	Fetal anomalies v0.1972	NSD2	Zornitza Stark Gene: nsd2 has been classified as Green List (High Evidence).
13 Jan 2022	Fetal anomalies v0.1972	NSD2	Zornitza Stark Classified gene: NSD2 as Green List (high evidence)
13 Jan 2022	Fetal anomalies v0.1972	NSD2	Zornitza Stark Gene: nsd2 has been classified as Green List (High Evidence).
13 Jan 2022	Fetal anomalies v0.1971	NSD2	Zornitza Stark gene: NSD2 was added gene: NSD2 was added to Fetal anomalies. Sources: Literature Mode of inheritance for gene: NSD2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: NSD2 were set to 30345613; 31171569 Phenotypes for gene: NSD2 were set to Rauch-Steindl syndrome, MIM# 619695 Review for gene: NSD2 was set to GREEN Added comment: 7 unrelated individuals reported with LOF variants. Gene thought to be responsible for many of the features of Wolf-Hirschorn syndrome. Prenatal growth retardation is a feature. Sources: Literature