Related gene-specific medical variations for Gene (Select 1641) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3358964	NM_001195553.2(DCX):c.575G>A (p.Arg192Gln)	DCX (R192Q +1 more)	Single nucleotide variant (missense variant)	Lissencephaly type 1 due to doublecortin gene mutation	GUncertain significance
Select item 3065092	NM_001195553.2(DCX):c.530T>G (p.Val177Gly)	DCX (V177G +1 more)	Single nucleotide variant (missense variant)	Lissencephaly type 1 due to doublecortin gene mutation	GUncertain significance
Select item 3065074	NM_001195553.2(DCX):c.604A>G (p.Lys202Glu)	DCX (K202E +1 more)	Single nucleotide variant (missense variant)	Lissencephaly type 1 due to doublecortin gene mutation	GUncertain significance
Select item 685828	GRCh37/hg19 Xq23(chrX:110531355-110561549)x3	DCX	Copy number gain	not provided	GUncertain significance
Select item 153209	GRCh38/hg38 Xq23(chrX:111318320-111348178)x3	DCX	Copy number gain	See cases	GPathogenic
Select item 144235	GRCh38/hg38 Xq23(chrX:111294396-111417260)x3	DCX	Copy number gain	See cases	GUncertain significance

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