"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "OLFML2B - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 780275	NM_015441.3(OLFML2B):c.1788T>C (p.Ala596=)	OLFML2B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 775620	NM_015441.3(OLFML2B):c.1047T>C (p.Pro349=)	OLFML2B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 791819	NM_015441.3(OLFML2B):c.1017C>T (p.Asn339=)	OLFML2B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1411942	NC_000001.10:g.(?_158581054)_(162750036_?)dup	LY9, MNDA +90 more	Duplication	Autoimmune interstitial lung disease-arthritis syndrome	GUncertain significance
Select item 1401040	NC_000001.10:g.(?_161816219)_(162040092_?)dup	ATF6, NOS1AP +1 more	Duplication	not provided	GUncertain significance
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	ARL8A, CNIH4 +956 more	Duplication	Gastrointestinal stromal tumor +2 more	GUncertain significance

ClinVar