DPP6

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red DPP6 in Mendeliome Version 1.3512	2 reviews	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 1.357	2 reviews	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 1.410	3 reviews	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	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category C gene Phenotypes Ventricular fibrillation, paroxysmal familial, 2
Red DPP6 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category C gene Expert Review Red Phenotypes Ventricular fibrillation, paroxysmal familial, 2

5 panels