| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Brugada syndrome v0.35 | RANGRF | Chirag Patel Marked gene: RANGRF as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Brugada syndrome v0.35 | RANGRF | Chirag Patel Gene: rangrf has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Brugada syndrome v0.35 | RANGRF |
Chirag Patel gene: RANGRF was added gene: RANGRF was added to Brugada syndrome. Sources: ClinGen refuted tags were added to gene: RANGRF. Mode of inheritance for gene: RANGRF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: RANGRF were set to Brugada syndrome, MONDO:0015263 Review for gene: RANGRF was set to RED Added comment: ClinGen REFUTED - Oct 2025 Sources: ClinGen |
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