"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "ATG16L2 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 781025	NM_033388.2(ATG16L2):c.956G>C (p.Cys319Ser)	ATG16L2 (C213S +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 787382	NM_014824.3(FCHSD2):c.1970C>T (p.Pro657Leu)	ATG16L2, FCHSD2 (P657L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2426953	NC_000011.9:g.(?_71146421)_(75283128_?)dup	ANAPC15, ARAP1 +63 more	Duplication	3-methylglutaconic aciduria, type VIIB	GUncertain significance

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