DPP6

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red DPP6 in Mendeliome Version 1.1891	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Intellectual disability, autosomal dominant 33 (MIM#616311) Tags SV/CNV disputed
Red DPP6 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.269	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Red Literature Phenotypes Intellectual disability, autosomal dominant 33 (MIM#616311) Tags SV/CNV disputed
Red DPP6 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 Red Genetic Health Queensland Phenotypes Intellectual disability, autosomal dominant 33 (MIM#616311) Tags disputed
Red DPP6 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category C gene Phenotypes Ventricular fibrillation, paroxysmal familial, 2
Red DPP6 in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category C gene Expert Review Red Phenotypes Ventricular fibrillation, paroxysmal familial, 2

5 panels