DIP2B

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
No list DIP2B 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 Removed Genetic Health Queensland Phenotypes Mental retardation, FRA12A type, MIM# 136630 Tags 5'UTR
Amber FRA12A STR in Mendeliome Version 1.1891	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Other Phenotypes Intellectual developmental disorder, autosomal dominant, FRA12A type MIM#136630 Tags 5'UTR
Amber FRA12A STR 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 Amber Other Phenotypes Mental retardation, FRA12A type MIM#136630 Tags 5'UTR
Amber FRA12A STR in Repeat Disorders Version 0.167	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes Mental retardation, FRA12A type MIM#136630 Tags paediatric-onset

4 panels