| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Congenital Heart Defect v0.502 | SCN5A | Chirag Patel Marked gene: SCN5A as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital Heart Defect v0.502 | SCN5A | Chirag Patel Gene: scn5a has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital Heart Defect v0.502 | SCN5A |
Chirag Patel gene: SCN5A was added gene: SCN5A was added to Congenital Heart Defect. Sources: ClinGen disputed tags were added to gene: SCN5A. Mode of inheritance for gene: SCN5A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: SCN5A were set to Congenital heart disease, MONDO:0005453 Review for gene: SCN5A was set to RED Added comment: ClinGen DISPUTED - Dec 2024 Sources: ClinGen |
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