"University of Washington Center for Mendelian Genomics, University of - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 691941	NM_014681.6(DHX34):c.466C>T (p.Gln156Ter)	DHX34 (Q156*)	Single nucleotide variant (nonsense)	Neurodevelopmental disorders +6 more	GLikely pathogenic
Select item 691940	NM_014681.6(DHX34):c.1322A>G (p.Asn441Ser)	DHX34 (N441S)	Single nucleotide variant (missense variant)	Microcephaly +5 more	GLikely pathogenic
Select item 691942	NM_014681.6(DHX34):c.2327G>C (p.Arg776Pro)	DHX34 (R776P)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder	GPathogenic

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