TNRC6B

Panel	Reviews	Mode of inheritance	Details
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Green TNRC6B in Autism Level 2: Neurology and neurodevelopmental disorders Version 0.198	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 1.1902	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 0.6063	review	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 1.0	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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