C1836602[trait identifier] AND "Johns Hopkins Genomics, Johns Hopkins - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 981531	NM_182943.3(PLOD2):c.2270A>T (p.Asp757Val)	PLOD2 (D736V +1 more)	Single nucleotide variant (missense variant)	Bruck syndrome 2	GUncertain significance
Select item 981530	NM_182943.3(PLOD2):c.778-6T>G	PLOD2	Single nucleotide variant (intron variant)	Bruck syndrome 2	GUncertain significance