"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "DLGAP1" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 788613	NM_004746.4(DLGAP1):c.2472C>T (p.Pro824=)	DLGAP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 727983	NM_004746.4(DLGAP1):c.2247T>C (p.His749=)	DLGAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 790190	NM_004746.4(DLGAP1):c.1977T>C (p.Ala659=)	DLGAP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 777265	NM_004746.4(DLGAP1):c.888G>A (p.Ser296=)	DLGAP1, DLGAP1-AS3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 771503	NM_004746.4(DLGAP1):c.852C>A (p.Thr284=)	DLGAP1, DLGAP1-AS3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1452047	NC_000018.9:g.(?_2847807)_(3582246_?)del	DLGAP1, EMILIN2 +5 more	Deletion	Holoprosencephaly 4	GPathogenic

ClinVar