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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 717838	NM_001017405.3(MAEA):c.309C>T (p.Ile103=)	MAEA	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 787794	NM_001017405.3(MAEA):c.333C>T (p.Ser111=)	MAEA	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 2424606	NC_000004.11:g.(?_493125)_(3495228_?)dup	FGFRL1, GAK +46 more	Duplication	Fibrous dysplasia of jaw	GUncertain significance
Select item 2422458	NC_000004.11:g.(?_493125)_(1843544_?)del	ATP5ME, CPLX1 +25 more	Deletion	not provided	GUncertain significance
Select item 1459277	NC_000004.11:g.(?_493125)_(2065854_?)del	ATP5ME, CPLX1 +29 more	Deletion	not provided	GPathogenic
Select item 1421534	NC_000004.11:g.(?_493125)_(3495228_?)del	DOK7, FAM193A +46 more	Deletion	Fibrous dysplasia of jaw	GUncertain significance

ClinVar