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| Genomic newborn screening: BabyScreen+ v2.0 | SCN3B | Gene migrated from ENSG00000166257 to ENSG00000166257 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | SCN3B |
Zornitza Stark gene: SCN3B was added gene: SCN3B was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: SCN3B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: SCN3B were set to Brugada syndrome |
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