"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "OR2B11" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 775699	NM_001004492.2(OR2B11):c.522G>A (p.Gly174=)	OR2B11	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 775700	NM_001004492.2(OR2B11):c.501G>C (p.Thr167=)	OR2B11	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1411294	NC_000001.10:g.(?_247599252)_(248059833_?)dup	OR2G3, OR2W3 +11 more	Duplication	Cryopyrin associated periodic syndrome	GUncertain significance
Select item 1003853	NC_000001.10:g.(?_247607254)_(247617036_?)dup	NLRP3, OR2B11	Duplication	Cryopyrin associated periodic syndrome	GUncertain significance
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	ARL8A, CNIH4 +956 more	Duplication	Gastrointestinal stromal tumor +2 more	GUncertain significance
Select item 830398	NC_000001.11:g.(?_247418775)_(247453734_?)dup	NLRP3, OR2B11	Duplication	Cryopyrin associated periodic syndrome	GUncertain significance

ClinVar