"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 263073	NM_182943.3(PLOD2):c.1500+12A>G	PLOD2	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 281238	NM_182943.3(PLOD2):c.652A>G (p.Ile218Val)	PLOD2 (I218V)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 263074	NM_182943.3(PLOD2):c.338+4G>A	PLOD2	Single nucleotide variant (intron variant)	Bruck syndrome 2 +2 more	GBenign

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