"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "PLA2G4D - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 790690	NM_178034.4(PLA2G4D):c.997C>T (p.Arg333Trp)	PLA2G4D (R333W)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 768702	NM_178034.4(PLA2G4D):c.943C>T (p.Leu315=)	PLA2G4D	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1024934	NC_000015.9:g.(?_32964879)_(91358519_?)dup	CGNL1, MAPDA +472 more	Duplication	Familial colorectal cancer +1 more	GUncertain significance

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