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| Genomic newborn screening: BabyScreen+ v2.0 | HCN4 | Gene migrated from ENSG00000138622 to ENSG00000138622 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | HCN4 |
Zornitza Stark gene: HCN4 was added gene: HCN4 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: HCN4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: HCN4 were set to Brugada syndrome |
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