"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LINGO1" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 779902	NM_032808.7(LINGO1):c.1830C>T (p.Asp610=)	LINGO1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 778558	NM_032808.7(LINGO1):c.1575C>T (p.Pro525=)	LINGO1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 776935	NM_032808.7(LINGO1):c.1557C>T (p.Pro519=)	LINGO1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 771195	NM_032808.7(LINGO1):c.1110G>A (p.Pro370=)	LINGO1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 757205	NM_032808.7(LINGO1):c.114G>A (p.Ser38=)	LINGO1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1024934	NC_000015.9:g.(?_32964879)_(91358519_?)dup	CGNL1, MAPDA +472 more	Duplication	Familial colorectal cancer +1 more	GUncertain significance

ClinVar