| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Brugada syndrome v0.44 | PKP2 | Chirag Patel Marked gene: PKP2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Brugada syndrome v0.44 | PKP2 | Chirag Patel Gene: pkp2 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Brugada syndrome v0.43 | PKP2 |
Chirag Patel gene: PKP2 was added gene: PKP2 was added to Brugada syndrome. Sources: ClinGen disputed tags were added to gene: PKP2. Mode of inheritance for gene: PKP2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: PKP2 were set to Brugada syndrome, MONDO:0015263 Review for gene: PKP2 was set to RED Added comment: ClinGen DISPUTED - Nov 2017 Sources: ClinGen |
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