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| Genomic newborn screening: BabyScreen+ v1.143 | MYLK | Zornitza Stark Marked gene: MYLK as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v1.143 | MYLK | Zornitza Stark Gene: mylk has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v1.143 | MYLK | Zornitza Stark Phenotypes for gene: MYLK were changed from Aortic aneurysm, familial thoracic 7 to Aortic aneurysm, familial thoracic 7, MIM#613780 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v1.142 | MYLK | Zornitza Stark changed review comment from: STRONG by ClinGen in terms of gene-disease relationship but not assessed for actionability yet.; to: STRONG by ClinGen in terms of gene-disease relationship but not assessed for actionability yet. Not suitable for gNBS. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v1.142 | MYLK | Zornitza Stark reviewed gene: MYLK: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Aortic aneurysm, familial thoracic 7, MIM#613780; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | MYLK2 |
Zornitza Stark gene: MYLK2 was added gene: MYLK2 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: MYLK2 was set to Unknown Phenotypes for gene: MYLK2 were set to Cardiomyopathy, hypertrophic |
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| Genomic newborn screening: BabyScreen+ v0.0 | MYLK |
Zornitza Stark gene: MYLK was added gene: MYLK was added to gNBS. Sources: Expert Review Amber,BabySeq Category B gene Mode of inheritance for gene: MYLK was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: MYLK were set to Aortic aneurysm, familial thoracic 7 |
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