| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Cardiac conduction disease v1.1 | NNT | Bryony Thompson Marked gene: NNT as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiac conduction disease v1.1 | NNT | Bryony Thompson Gene: nnt has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiac conduction disease v1.1 | NNT |
Bryony Thompson gene: NNT was added gene: NNT was added to Cardiac conduction disease. Sources: Literature Mode of inheritance for gene: NNT was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: NNT were set to 26025024 Phenotypes for gene: NNT were set to left ventricular noncompaction MONDO:0018901 Review for gene: NNT was set to RED Added comment: Only a single publication reporting an association with LVNC from 2015. Biallelic variants cause a mitochondrial disease that was first reported in 2012; therefore, more evidence of an association with LVNC would be expected. Sources: Literature |
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