C1836602[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1705607	NM_182943.3(PLOD2):c.1958C>G (p.Pro653Arg)	PLOD2 (P632R +1 more)	Single nucleotide variant (missense variant)	Bruck syndrome 2 +1 more	GConflicting classifications of pathogenicity
Select item 1444936	NM_182943.3(PLOD2):c.1045A>G (p.Lys349Glu)	PLOD2 (K349E)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity