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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 761640	NM_000594.4(TNF):c.39C>A (p.Ala13=)	TNF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 784495	NM_000594.4(TNF):c.87G>T (p.Arg29=)	TNF	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781865	NM_000594.4(TNF):c.251C>T (p.Pro84Leu)	TNF (P84L)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 748239	NM_000594.4(TNF):c.354G>A (p.Glu118=)	TNF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 723481	NM_000594.4(TNF):c.477C>T (p.Ile159=)	TNF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 732409	NM_000594.4(TNF):c.489C>T (p.Tyr163=)	TNF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2427350	NC_000006.11:g.(?_30695893)_(36953949_?)dup	ABHD16A, AGER +172 more	Duplication	Proteasome-associated autoinflammatory syndrome 1	GUncertain significance
Select item 2424220	NC_000006.11:g.(?_30695893)_(31937492_?)dup	ABHD16A, AIF1 +63 more	Duplication	not provided	GUncertain significance

ClinVar