C4551985[trait identifier] AND "Victorian Clinical Genetics Services, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 870410	NM_006208.3(ENPP1):c.1769G>A (p.Ser590Asn)	ENPP1 (S590N)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 870422	NM_006208.3(ENPP1):c.2376T>A (p.Asn792Lys)	ENPP1 (N792K)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity