"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LGALS4" - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 777529	NM_006149.4(LGALS4):c.47C>T (p.Thr16Met)	LGALS4 (T16M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 712328	NM_006149.4(LGALS4):c.6C>T (p.Ala2=)	LGALS4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2424211	NC_000019.9:g.(?_39205089)_(40913839_?)dup	ACP7, ACTN4 +53 more	Duplication	not provided	GUncertain significance
Select item 2423269	NC_000019.9:g.(?_38375572)_(39738787_?)dup	DPF1, ECH1 +34 more	Duplication	RYR1-related disorder	GUncertain significance

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