C4748184[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 717059	NM_004618.5(TOP3A):c.2317A>G (p.Asn773Asp)	TOP3A (N678D +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 787133	NM_004618.5(TOP3A):c.315-4C>G	TOP3A	Single nucleotide variant (intron variant)	Microcephaly, growth restriction, and increased sister chromatid exchange 2 +2 more	GBenign
Select item 1573144	NM_004618.5(TOP3A):c.180+10C>G	TOP3A	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign

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