SAG

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green SAG in Mendeliome Version 1.4216	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Oguchi disease-1, MIM# 258100 Retinitis pigmentosa 47, autosomal recessive MIM# 613758 Retinitis pigmentosa 96, autosomal dominant, MIM# 620228
Amber SAG in Retinitis pigmentosa Level 2: Ophthalmological disorders Version 0.238 Component of the following Super Panels: Retinal Disorders Superpanel	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Amber Royal Melbourne Hospital Phenotypes Retinitis pigmentosa 47, autosomal recessive MIM# 613758 Retinitis pigmentosa 96, autosomal dominant, MIM# 620228 Tags founder
Green SAG in Congenital Stationary Night Blindness Level 2: Ophthalmological disorders Version 0.24 Component of the following Super Panels: Retinal Disorders Superpanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Oguchi disease-1, MIM# 258100
Red SAG in Congenital nystagmus Level 2: Ophthalmological disorders Version 1.24	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Royal Melbourne Hospital Phenotypes Oguchi disease-1, MIM# 258100

4 panels