ClinVar for MedGen (Select 1673088) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2440812	NM_001933.5(DLST):c.911A>G (p.Asp304Gly)	DLST (D304G)	Single nucleotide variant (missense variant +1 more)	Paragangliomas 7	GUncertain significance
Select item 635133	NM_001933.5(DLST):c.1121G>A (p.Gly374Glu)	DLST (G374E)	Single nucleotide variant (missense variant +1 more)	Paragangliomas 7	GPathogenic