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Fetal anomalies v0.4501 RAD21 Zornitza Stark Marked gene: RAD21 as ready
Fetal anomalies v0.4501 RAD21 Zornitza Stark Gene: rad21 has been classified as Green List (High Evidence).
Fetal anomalies v0.4501 RAD21 Zornitza Stark Phenotypes for gene: RAD21 were changed from COHESINOPATHY to Cornelia de Lange syndrome 4, MIM# 614701; Holoprosencephaly
Fetal anomalies v0.4500 RAD21 Zornitza Stark Publications for gene: RAD21 were set to
Fetal anomalies v0.4499 RAD21 Zornitza Stark Mode of inheritance for gene: RAD21 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Fetal anomalies v0.0 RAD21 Zornitza Stark gene: RAD21 was added
gene: RAD21 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: RAD21 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: RAD21 were set to COHESINOPATHY