| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Additional findings_Paediatric v1.0 | ACVR2B | Gene migrated from ENSG00000114739 to ENSG00000114739 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | ACVR2B |
Zornitza Stark gene: ACVR2B was added gene: ACVR2B was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: ACVR2B was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ACVR2B were set to Left-right axis malformation |
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