Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Hereditary Melanoma Panel (7 genes)	CDKN2A, CDK4, POT1, TERT, TERF2IP, BAP1, MITF	Hereditary Melanoma Panel (7 genes) - ULG	Familial melanoma	Centre de Génétique Humaine - CHU Sart-Tilman
Waardenburg syndrome (gene panel)	EDN3, EDNRB, MITF, PAX3, SNAI2, SOX10	Waardenburg syndrome (6 genes) - UZA	Waardenburg syndrome type 1, Waardenburg syndrome type 2, Waardenburg syndrome type 3, Waardenburg-Shah syndrome	Centrum Medische Genetica - UZ Antwerpen
Melanoma (6 genes)	BAP1, CDK4, CDKN2A, MC1R, MITF, POT1	Melanoma (6 genes) - UCL	Familial melanoma, MITF-related melanoma and renal cell carcinoma predisposition syndrome, Uveal melanoma, Melanoma of soft tissue	Centre de Génétique Médicale UCL
Paraganglioma-pheochromocytoma (gene panel)	SDHA, SDHB, SDHC, SDHD, SDHAF2, RET, VHL, NF1	Paraganglioma-pheochromocytoma (7 genes) - KUL	Hereditary pheochromocytoma-paraganglioma	Centrum Menselijke Erfelijkheid - KUL
Pheochromocytoma - paraganglioma syndrome (gene panel)	SDHB, SDHC, SDHD, SDHA, MAX, TMEM127, SDHAF2, VHL, RET, SUCLG2	Pheochromocytoma - paraganglioma syndrome - UGent	Hereditary pheochromocytoma-paraganglioma	Centrum Medische Genetica - UZ Gent
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
Uniparental disomy	7p12.1, 7q32.2		Silver-Russell syndrome	Centre de Génétique Médicale UCL

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