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| Additional findings_Paediatric v1.0 | AKAP9 | Gene migrated from ENSG00000127914 to ENSG00000127914 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | AKAP9 |
Zornitza Stark gene: AKAP9 was added gene: AKAP9 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: AKAP9 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: AKAP9 were set to Long QT syndrome |
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