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)
Beckwith-Wiedemann syndrome (11p15 methylation)	H19, KCNQ1OT1, IGF2		Beckwith-Wiedemann syndrome due to imprinting defect of 11p15, Beckwith-Wiedemann syndrome	Centrum Menselijke Erfelijkheid - KUL
Obesity (gene panel)	ADCY3, BDNF, LEP, LEPR, MC3R, MC4R, NR0B2, NTRK2, PCSK1, POMC, SIM1, UCP3	Obesitas (genepanel) - UZA		Centrum Medische Genetica - UZ Antwerpen
Obesitas, early onset (gene panel)	MC4R, MC3R, LEP, LEPR, PCSK1, POMC, SIM1, NTRK2	Obesitas, early onset (8 genes) - VUB		Centrum Medische Genetica - UZ Brussel VUB
Obesitas, Monogenic early onset	MC4R		Obesity due to melanocortin 4 receptor deficiency	Centre de Génétique Humaine - CHU Sart-Tilman
Beckwith-Wiedemann syndrome	11p15.5		Beckwith-Wiedemann syndrome due to imprinting defect of 11p15, Beckwith-Wiedemann syndrome due to 11p15 microdeletion	Centre de Génétique Médicale UCL
Silver-Russell syndrome	11p15.5, 7p12.1, 7q32.2		Silver-Russell syndrome, Silver-Russell syndrome due to an imprinting defect of 11p15, Silver-Russell syndrome due to 11p15 microduplication	Centre de Génétique Médicale UCL

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