"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "ADRB2"[ - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 17742	NM_000024.6(ADRB2):c.46= (p.Gly16=)	ADRB2, LOC129994952 (R16G)	Single nucleotide variant (no sequence alteration)	not provided	GBenign
Select item 703863	NM_000024.6(ADRB2):c.66C>T (p.His22=)	ADRB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 17743	NM_000024.6(ADRB2):c.79= (p.Glu27=)	ADRB2 (Q27E)	Single nucleotide variant (no sequence alteration)	not provided	GBenign
Select item 706311	NM_000024.6(ADRB2):c.206A>G (p.Asn69Ser)	ADRB2 (N69S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 746540	NM_000024.6(ADRB2):c.276C>G (p.Ala92=)	ADRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 757511	NM_000024.6(ADRB2):c.492C>A (p.Thr164=)	ADRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 704039	NM_000024.6(ADRB2):c.560A>G (p.Asn187Ser)	ADRB2 (N187S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 703951	NM_000024.6(ADRB2):c.659C>G (p.Ser220Cys)	ADRB2 (S220C)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 784824	NM_000024.6(ADRB2):c.771A>T (p.Gly257=)	ADRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 785003	NM_000024.6(ADRB2):c.990A>C (p.Pro330=)	ADRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 704695	NM_000024.6(ADRB2):c.1098T>C (p.Tyr366=)	ADRB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 704273	NM_000024.6(ADRB2):c.1179T>C (p.Thr393=)	ADRB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2425319	NC_000005.9:g.(?_147774340)_(149681936_?)del	ABLIM3, ADRB2 +23 more	Deletion	not provided	GUncertain significance
Select item 457359	NC_000005.9:g.(?_86400000)_(154000000_?)del	CCDC69, CCNH +385 more	Deletion	Familial adenomatous polyposis 1 +1 more	GPathogenic