| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Brugada syndrome v0.44 | SCN2B | Chirag Patel Marked gene: SCN2B as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Brugada syndrome v0.44 | SCN2B | Chirag Patel Gene: scn2b has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Brugada syndrome v0.43 | SCN2B |
Chirag Patel gene: SCN2B was added gene: SCN2B was added to Brugada syndrome. Sources: ClinGen disputed tags were added to gene: SCN2B. Mode of inheritance for gene: SCN2B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: SCN2B were set to Brugada syndrome, MONDO:0015263 Review for gene: SCN2B was set to RED Added comment: ClinGen DISPUTED - Nov 2017 Sources: ClinGen |
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