SLC6A17

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Amber SLC6A17 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Mental retardation, autosomal recessive 48, MIM# 616269
Amber SLC6A17 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Genetic Health Queensland Phenotypes Mental retardation, autosomal recessive 48, MIM# 616269
Red SLC6A17 in Fetal anomalies Version 1.255	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Genomics England PanelApp Phenotypes Mental retardation, autosomal recessive 48, MIM# 616269

3 panels