"Fulgent Genetics, Fulgent Genetics"[submitter] AND "DNHD1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 774620	NM_144666.3(DNHD1):c.2839G>T (p.Glu947Ter)	DNHD1 (E947*)	Single nucleotide variant (nonsense)	Spermatogenic failure 65 +2 more	GBenign/Likely benign
Select item 742167	NM_144666.3(DNHD1):c.4060G>A (p.Ala1354Thr)	DNHD1 (A1354T)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign