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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 781371	NM_006151.3(LPO):c.30C>G (p.Leu10=)	LPO	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 783793	NM_006151.3(LPO):c.164+9_164+12del	LPO	Deletion (intron variant)	not provided	GBenign
Select item 770270	NM_006151.3(LPO):c.164+9G>C	LPO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 781372	NM_006151.3(LPO):c.314C>T (p.Thr105Ile)	LPO (T105I)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign
Select item 790724	NM_006151.3(LPO):c.1032G>T (p.Leu344=)	LPO	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 712294	NM_006151.3(LPO):c.1122A>C (p.Ser374=)	LPO	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 781308	NM_006151.3(LPO):c.1931+10T>C	LPO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1412084	NC_000017.10:g.(?_54671585)_(59938900_?)dup	USP32, VEZF1 +54 more	Duplication	Familial aplasia of the vermis +1 more	GUncertain significance

ClinVar