| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Hypertrophic cardiomyopathy v2.0 | SVIL | Gene migrated from ENSG00000197321 to ENSG00000197321 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hypertrophic cardiomyopathy v1.23 | Sarah Milton Copied gene SVIL from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hypertrophic cardiomyopathy v1.23 | SVIL |
Sarah Milton gene: SVIL was added gene: SVIL was added to Hypertrophic cardiomyopathy. Sources: Expert Review Amber,Literature Mode of inheritance for gene: SVIL was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SVIL were set to 32779703 Phenotypes for gene: SVIL were set to Myofibrillar myopathy, MIM#619040 Penetrance for gene: SVIL were set to unknown |
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