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  • Molecular assay reagents intended to identify deletions or duplications of the von Hippel-Lindau tumor suppressor (VHL) gene, located at chromosome 3p25.3, which encodes the protein von Hippel-Lindau disease tumor suppressor. Genetic variants at this locus have been associated with familial erythrocytosis, pheochromocytoma, renal cell carcinoma, and von Hippel-Lindau syndrome.
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