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| Paediatric disorders - additional genes v0.26 | ACVR2B | Helen Brittain Classified gene: ACVR2B as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Paediatric disorders - additional genes v0.26 | ACVR2B | Helen Brittain Added comment: Comment on list classification: Meets criteria for green rating under 100K - awaiting higher level sign off re GMS indication | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Paediatric disorders - additional genes v0.26 | ACVR2B | Helen Brittain Gene: acvr2b has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Paediatric disorders - additional genes v0.25 | ACVR2B |
Helen Brittain gene: ACVR2B was added gene: ACVR2B was added to Paediatric disorders - additional genes. Sources: Literature Mode of inheritance for gene: ACVR2B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: ACVR2B were set to 9916847 Phenotypes for gene: ACVR2B were set to Heterotaxy syndrome Heterotaxy, visceral, 4, autosomal, 613751 Review for gene: ACVR2B was set to GREEN Added comment: Three unrelated cases of left-right axis malformations, including cardiac anomalies e.g. left atrial isomerism Sources: Literature |
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