"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "WWC1"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 732367	NM_015238.3(WWC1):c.838G>A (p.Val280Met)	WWC1 (V280M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 751795	NM_015238.3(WWC1):c.1002G>T (p.Leu334=)	WWC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 790569	NM_015238.3(WWC1):c.1153C>A (p.Arg385=)	WWC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 756633	NM_015238.3(WWC1):c.1471G>A (p.Gly491Ser)	WWC1 (G491S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 771387	NM_015238.3(WWC1):c.1902C>T (p.Tyr634=)	WWC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 710265	NM_015238.3(WWC1):c.1911C>T (p.Ser637=)	WWC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2425244	NC_000005.9:g.(?_167849013)_(169661202_?)del	C5orf58, DOCK2 +8 more	Deletion	DOCK2 deficiency	GPathogenic

ClinVar