Related gene-specific medical variations for Gene (Select 9416) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2664152	NM_004818.3(DDX23):c.2437C>T (p.Arg813Cys)	DDX23 (R813C)	Single nucleotide variant (missense variant)	Congenital bilateral perisylvian syndrome	GLikely pathogenic
Select item 2576074	NM_004818.3(DDX23):c.779A>G (p.Lys260Arg)	DDX23 (K260R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1676504	NM_004818.3(DDX23):c.1493G>T (p.Arg498Leu)	DDX23 (R498L)	Single nucleotide variant	not provided	GUncertain significance

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