"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LOC1300 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 663413	NC_000018.9:g.(?_55225777)_(56940458_?)dup	LOC130062566, LOC130062567 +87 more	Duplication	not provided	GUncertain significance
Select item 1667999	NM_000140.5(FECH):c.68-20G>A	FECH, LOC130062555	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 550	NM_000140.5(FECH):c.68-23C>T	FECH, LOC130062555	Single nucleotide variant (intron variant)	Protoporphyria, erythropoietic, 1 +1 more	GConflicting classifications of pathogenicity

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