"Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic C - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2429038	NM_001278716.2(FBXL4):c.1389+269G>A	FBXL4	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2429040	NM_001278716.2(FBXL4):c.513-3C>A	FBXL4	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 437490	NM_001278716.2(FBXL4):c.292C>T (p.Arg98Ter)	FBXL4 (R98*)	Single nucleotide variant (nonsense +1 more)	not provided +1 more	GPathogenic/Likely pathogenic

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