C3150658[trait identifier] AND "Mendelics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 802829	NM_030653.4(DDX11):c.1699C>G (p.Gln567Glu)	DDX11 (Q541E +1 more)	Single nucleotide variant (missense variant)	Warsaw breakage syndrome	GBenign
Select item 802830	NM_030653.4(DDX11):c.1819G>C (p.Ala607Pro)	DDX11 (A607P +1 more)	Single nucleotide variant (missense variant)	Warsaw breakage syndrome	GLikely benign
Select item 802831	NM_030653.4(DDX11):c.2572G>A (p.Val858Ile)	DDX11 (V858I +3 more)	Single nucleotide variant (missense variant)	Warsaw breakage syndrome	GBenign

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