"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "FEM1B"[ - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 779892	NM_015322.5(FEM1B):c.39C>T (p.Ser13=)	FEM1B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1464977	NM_015322.5(FEM1B):c.599T>C (p.Ile200Thr)	FEM1B (I200T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1512687	NC_000015.9:g.(?_66161924)_(69018313_?)dup	AAGAB, C15orf61 +21 more	Duplication	Neuronal ceroid lipofuscinosis	GUncertain significance
Select item 1024934	NC_000015.9:g.(?_32964879)_(91358519_?)dup	CGNL1, MAPDA +472 more	Duplication	Familial colorectal cancer +1 more	GUncertain significance

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