"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "MAPK12" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 720967	NM_002969.6(MAPK12):c.182C>T (p.Pro61Leu)	MAPK12 (P61L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2426562	NC_000022.10:g.(?_50659287)_(50697352_?)del	HDAC10, MAPK12 +1 more	Deletion	not provided	GPathogenic
Select item 2425301	NC_000022.10:g.(?_50297486)_(51066207_?)del	ADM2, ALG12 +29 more	Deletion	not provided	GPathogenic
Select item 2423149	NC_000022.10:g.(?_50167881)_(51066207_?)del	CHKB, ARSA +31 more	Deletion	not provided	GPathogenic
Select item 1441357	NC_000022.10:g.(?_50167881)_(51066207_?)dup	ADM2, ALG12 +31 more	Duplication	ALG12-congenital disorder of glycosylation	GUncertain significance
Select item 1071720	NC_000022.10:g.(?_50297466)_(51066227_?)del	ADM2, ALG12 +29 more	Deletion	ALG12-congenital disorder of glycosylation	GPathogenic
Select item 831877	NC_000022.11:g.(?_50225794)_(50255881_?)dup	MAPK12, HDAC10 +1 more	Duplication	not provided	GUncertain significance

ClinVar