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Mendeliome v1.4221 SCN1B Zornitza Stark reviewed gene: SCN1B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Brugada syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v1.4221 SCN1B Zornitza Stark Marked gene: SCN1B as ready
Mendeliome v1.4221 SCN1B Zornitza Stark Gene: scn1b has been classified as Green List (High Evidence).
Mendeliome v1.4221 Zornitza Stark Copied gene SCN1B from panel Genetic Epilepsy
Mendeliome v1.4221 SCN1B Zornitza Stark gene: SCN1B was added
gene: SCN1B was added to Mendeliome. Sources: Expert Review Green,Victorian Clinical Genetics Services,Australian Genomics Health Alliance Epilepsy Flagship
Mode of inheritance for gene: SCN1B was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: SCN1B were set to 19710327; 28218389; 23148524
Phenotypes for gene: SCN1B were set to Developmental and epileptic encephalopathy (MONDO:0100062); generalized epilepsy with febrile seizures plus (MONDO:0018214)