"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "TNFAIP8 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 723112	NM_024575.5(TNFAIP8L2):c.71G>A (p.Arg24His)	LYSMD1, TNFAIP8L2 +1 more (R24H)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 775139	NM_024575.5(TNFAIP8L2):c.363C>G (p.Thr121=)	LYSMD1, TNFAIP8L2 +1 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 708675	NM_024575.5(TNFAIP8L2):c.408G>A (p.Thr136=)	LYSMD1, TNFAIP8L2 +1 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1445481	NC_000001.10:g.(?_149895434)_(156851434_?)dup	CKS1B, PRCC +228 more	Duplication	MHC class II deficiency +3 more	GUncertain significance
Select item 1023952	NC_000001.10:g.(?_151122490)_(151585008_?)dup	CGN, LYSMD1 +14 more	Duplication	Severe myoclonic epilepsy in infancy	GUncertain significance
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	ARL8A, CNIH4 +956 more	Duplication	Gastrointestinal stromal tumor +2 more	GUncertain significance

ClinVar