"Mendelics"[submitter] AND "MAX"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1042009	NM_002382.5(MAX):c.429G>C (p.Glu143Asp)	MAX (E80D +4 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 803032	NM_002382.5(MAX):c.172-6230G>A	MAX (V69I +1 more)	Single nucleotide variant (synonymous variant +2 more)	Pheochromocytoma +1 more	GConflicting classifications of pathogenicity