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| Additional findings_Paediatric v1.0 | SLC11A2 | Gene migrated from ENSG00000110911 to ENSG00000110911 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | SLC11A2 |
Zornitza Stark gene: SLC11A2 was added gene: SLC11A2 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: SLC11A2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SLC11A2 were set to Anemia, hypochromic microcytic |
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