C1864652[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 259250	NM_004247.4(EFTUD2):c.1058+3_1058+7del	EFTUD2	Deletion (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 30400	NM_004247.4(EFTUD2):c.784C>T (p.Arg262Trp)	EFTUD2 (R262W +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic
Select item 259251	NM_004247.4(EFTUD2):c.106-17C>T	EFTUD2	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign

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