| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Transplant Co-Morbidity v1.0 | APOC2 | Gene migrated from ENSG00000234906 to ENSG00000234906 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Transplant Co-Morbidity v0.0 | APOC2 |
Bryony Thompson gene: APOC2 was added gene: APOC2 was added to Transplant Co-Morbidity Superpanel. Sources: Royal Melbourne Hospital,Expert Review Green Mode of inheritance for gene: APOC2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: APOC2 were set to 32280258; 32292609; PMID: 32562799; 26044956 Phenotypes for gene: APOC2 were set to Hyperlipoproteinemia, type Ib MIM#207750 |
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