Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Bronchiectasis (4 genes)	CFTR, SCNN1A, SCNN1B, SCNN1G	Bronchiectasis (4 genes) - UCL	Idiopathic bronchiectasis	Centre de Génétique Médicale UCL
Bronchiectasies with or without elevated sweat chloride panel (5 genes)	CFTR, SCNN1A, SCNN1B, SCNN1G	Pulmonary/Bronchiectasies (5 genes) - IPG	Idiopathic bronchiectasis, Cystic fibrosis	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Lipodystrophy (2 genes)	AGPAT2, BSCL2	Lipodystrophy (2 genes) - IPG	Congenital generalized lipodystrophy, Severe neurodegenerative syndrome with lipodystrophy	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Congenital generalized lipodystrophy type 2 / Spastic paraplegia-17 / Hereditary motor neuronopathy type VA / Silver spastic paraplegia syndrome (hot spot mutation - p.Asn88Ser; p.Ser90; p.Arg96His)	BSCL2		Autosomal dominant spastic paraplegia type 17, Severe neurodegenerative syndrome with lipodystrophy, Distal hereditary motor neuropathy type 5, Congenital generalized lipodystrophy	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Alport autosomal recessive and X-linked and hematuria (3 genes)	COL4A3, COL4A4, COL4A5	Alport (X-linked and recessive) (3 genes) - IPG	Autosomal recessive Alport syndrome, X-linked Alport syndrome	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
CYP3A4*22 genotyping - drug metabolism - Pharmacogenetics	CYP3A4		Tacrolimus dose selection	Centre de Génétique Médicale UCL

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