"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 496154	NM_002317.7(LOX):c.740+6G>A	LOX, SRFBP1	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 1285026	NM_002317.7(LOX):c.643C>T (p.Leu215=)	LOX, SRFBP1	Single nucleotide variant (5 prime UTR variant +2 more)	Cardiovascular phenotype +1 more	GLikely benign