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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 308015	NM_002300.8(LDHB):c.879A>G (p.Pro293=)	LDHB	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 745038	NM_002300.8(LDHB):c.726C>T (p.Val242=)	LDHB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 725612	NM_002300.8(LDHB):c.435G>A (p.Thr145=)	LDHB	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 308027	NM_002300.8(LDHB):c.130-3_130-2del	LDHB	Deletion (splice acceptor variant)	not provided +1 more	GBenign/Likely benign
Select item 2423437	NC_000012.11:g.(?_20522219)_(22089608_?)dup	ABCC9, GOLT1B +13 more	Duplication	not provided	GUncertain significance
Select item 1445073	NC_000012.11:g.(?_21590665)_(22089608_?)dup	ABCC9, GOLT1B +6 more	Duplication	Dilated cardiomyopathy 1O	GUncertain significance
Select item 1411401	NC_000012.11:g.(?_21590665)_(22089608_?)del	ABCC9, GOLT1B +6 more	Deletion	Dilated cardiomyopathy 1O	GUncertain significance

ClinVar