"Genome-Nilou Lab"[submitter] AND "PLOD2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 343643	NM_182943.3(PLOD2):c.*37A>G	PLOD2	Single nucleotide variant (3 prime UTR variant)	Bruck syndrome 2 +1 more	GBenign
Select item 674931	NM_182943.3(PLOD2):c.2121+26A>G	PLOD2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1291877	NM_182943.3(PLOD2):c.680-45C>T	PLOD2	Single nucleotide variant (intron variant)	Bruck syndrome 2 +1 more	GBenign
Select item 674924	NM_182943.3(PLOD2):c.503-47T>C	PLOD2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 674922	NM_182943.3(PLOD2):c.339-22dup	PLOD2	Duplication (intron variant)	Bruck syndrome 2 +1 more	GBenign
Select item 263074	NM_182943.3(PLOD2):c.338+4G>A	PLOD2	Single nucleotide variant (intron variant)	Bruck syndrome 2 +2 more	GBenign

ClinVar