"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "SEC62"[ - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 767941	NM_003262.4(SEC62):c.75C>G (p.Ala25=)	SEC62	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 775924	NM_003262.4(SEC62):c.282C>G (p.Ala94=)	SEC62	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2422930	NC_000003.11:g.(?_168802697)_(172835521_?)dup	ACTRT3, CLDN11 +25 more	Duplication	Fanconi-Bickel syndrome	GUncertain significance
Select item 1390486	NC_000003.11:g.(?_169482388)_(170130102_?)dup	ACTRT3, GPR160 +10 more	Duplication	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance

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