"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "GOLGA4" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 710917	NM_002078.5(GOLGA4):c.173C>T (p.Thr58Ile)	GOLGA4 (T58I +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 719408	NM_002078.5(GOLGA4):c.1796A>T (p.Asn599Ile)	GOLGA4 (N599I +5 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 710918	NM_002078.5(GOLGA4):c.4655A>G (p.Asn1552Ser)	GOLGA4, LOC129389056 (N1552S +5 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 787012	NM_002078.5(GOLGA4):c.5782C>G (p.Leu1928Val)	GOLGA4 (L1928V +5 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 156204	NM_002078.5(GOLGA4):c.6174A>T (p.Arg2058Ser)	GOLGA4 (R2080S +5 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 778066	NM_002078.5(GOLGA4):c.6396+9C>T	GOLGA4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3246806	NC_000003.11:g.(?_37067426)_(37502150_?)del	APRG1, GOLGA4 +3 more	Deletion	Hereditary nonpolyposis colorectal neoplasms	GPathogenic
Select item 1455527	NC_000003.11:g.(?_16710965)_(41275270_?)del	ACAA1, ACVR2B +93 more	Deletion	not provided	GPathogenic
Select item 1373543	NC_000003.11:g.(?_37034542)_(38835501_?)dup	ACAA1, ACVR2B +19 more	Duplication	Heterotaxy, visceral, 4, autosomal	GUncertain significance

ClinVar