"Genome Diagnostics Laboratory, Amsterdam University Medical Center"[s - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 516236	NM_006767.4(LZTR1):c.320+12C>T	LZTR1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 496332	NM_006767.4(LZTR1):c.1209C>T (p.Phe403=)	LZTR1	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign/Likely benign
Select item 516186	NM_006767.4(LZTR1):c.1530C>T (p.His510=)	LZTR1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 1109493	NM_006767.4(LZTR1):c.1563C>T (p.Phe521=)	LZTR1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GBenign/Likely benign
Select item 379653	NM_006767.4(LZTR1):c.2160C>T (p.Phe720=)	LZTR1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 516329	NM_006767.4(LZTR1):c.2219+13C>T	LZTR1	Single nucleotide variant (intron variant)	not specified +3 more	GBenign

ClinVar