C1970506[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 536823	NM_016616.5(NME8):c.1657C>T (p.Arg553Ter)	NME8 (R553*)	Single nucleotide variant (nonsense)	Primary ciliary dyskinesia 6	GUncertain significance
Select item 409675	NM_016616.5(NME8):c.1684A>G (p.Lys562Glu)	NME8 (K562E)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia 6	GUncertain significance
Select item 580084	NM_016616.5(NME8):c.1735A>G (p.Asn579Asp)	NME8 (N579D)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia 6 +1 more	GUncertain significance

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