"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "PLCB2"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 778527	NM_004573.3(PLCB2):c.3113+10C>T	PLCB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 795986	NM_004573.3(PLCB2):c.2516del (p.Gly839fs)	PLCB2 (G835fs +1 more)	Deletion (frameshift variant)	not provided	GBenign
Select item 733612	NM_004573.3(PLCB2):c.1746T>C (p.Tyr582=)	PLCB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 776873	NM_004573.3(PLCB2):c.1722G>A (p.Ser574=)	PLCB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 727553	NM_004573.3(PLCB2):c.1412C>T (p.Thr471Ile)	PLCB2 (T471I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 769411	NM_004573.3(PLCB2):c.936C>G (p.His312Gln)	PLCB2 (H312Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3243779	NC_000015.9:g.(?_38545387)_(42105565_?)dup	ANKRD63, BAHD1 +49 more	Duplication	Mosaic variegated aneuploidy syndrome 1	GUncertain significance
Select item 1024934	NC_000015.9:g.(?_32964879)_(91358519_?)dup	CGNL1, MAPDA +472 more	Duplication	Familial colorectal cancer +1 more	GUncertain significance

ClinVar