"PreventionGenetics, part of Exact Sciences"[submitter] AND "DCX"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040860	NM_001195553.2(DCX):c.1044+4T>C	DCX	Single nucleotide variant (intron variant)	DCX-related condition	GLikely benign
Select item 262927	NM_001195553.2(DCX):c.947-46T>C	DCX	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 2631966	NM_001195553.2(DCX):c.904C>T (p.Arg302Cys)	DCX (R302C +1 more)	Single nucleotide variant (missense variant)	DCX-related condition	GUncertain significance
Select item 262926	NM_001195553.2(DCX):c.705+48A>G	DCX	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 262925	NM_001195553.2(DCX):c.705+29G>A	DCX	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 158486	NM_001195553.2(DCX):c.588T>C (p.Arg196=)	DCX	Single nucleotide variant (synonymous variant)	DCX-related condition +3 more	GBenign/Likely benign
Select item 384621	NM_001195553.2(DCX):c.96C>T (p.Ser32=)	DCX	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 3054266	NM_001195553.2(DCX):c.-22-395G>A	DCX (E54K)	Single nucleotide variant (missense variant +1 more)	DCX-related condition	GLikely benign
Select item 3046001	NM_001195553.2(DCX):c.-22-558T>G	DCX	Single nucleotide variant (5 prime UTR variant +1 more)	DCX-related condition	GLikely benign

ClinVar