TNRC6B

Panel	Reviews	Mode of inheritance	Details
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Green TNRC6B in Autism Level 2: Neurology and neurodevelopmental disorders Version 0.224	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Global developmental delay with speech and behavioural abnormalities, MIM# 619243
Green TNRC6B in Mendeliome Version 1.3512	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Global developmental delay with speech and behavioural abnormalities, MIM# 619243
Green TNRC6B in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.410	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genetic Health Queensland Victorian Clinical Genetics Services Phenotypes Global developmental delay with speech and behavioural abnormalities, MIM# 619243
Amber TNRC6B in Speech apraxia Level 2: Neurology and neurodevelopmental disorders Version 1.27	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert Review Expert list Phenotypes Global developmental delay with speech and behavioral abnormalities, MIM# 619243

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