"Genome Diagnostics Laboratory, Amsterdam University Medical Center"[s - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 496156	NM_002382.5(MAX):c.37-15del	MAX	Deletion (intron variant)	Hereditary pheochromocytoma-paraganglioma +1 more	GBenign/Likely benign
Select item 1174781	NM_002382.5(MAX):c.36+11G>C	LOC130055850, MAX	Single nucleotide variant (intron variant)	Hereditary pheochromocytoma-paraganglioma +1 more	GLikely benign