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| Additional findings_Paediatric v1.0 | SMAD6 | Gene migrated from ENSG00000137834 to ENSG00000137834 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | SMAD6 |
Zornitza Stark gene: SMAD6 was added gene: SMAD6 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: SMAD6 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: SMAD6 were set to Cardiovascular malformation, congenital |
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