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| Additional findings_Paediatric v1.0 | SCN5A | Gene migrated from ENSG00000183873 to ENSG00000183873 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | SCN5A | Zornitza Stark Added phenotypes Brugada syndrome for gene: SCN5A | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | SCN5A |
Zornitza Stark gene: SCN5A was added gene: SCN5A was added to Newborn Screening_BabySeq. Sources: BabySeq Category B gene,Expert Review Amber Mode of inheritance for gene: SCN5A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: SCN5A were set to Long QT syndrome |
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