| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Transplant Co-Morbidity Superpanel v0.0 | FGA |
Bryony Thompson gene: FGA was added gene: FGA was added to Transplant Co-Morbidity Superpanel. Sources: Victorian Clinical Genetics Services,Expert Review Green Mode of inheritance for gene: FGA was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: FGA were set to 17295221; 11739173; 19073821; 31064749 Phenotypes for gene: FGA were set to Afibrinogenemia, congenital (MIM#202400) |
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