List of variants in gene DCX reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_001195553.2(DCX):c.167G>T (p.Arg56Leu)	rs587783525
NM_001195553.2(DCX):c.263C>T (p.Thr88Met)
NM_001195553.2(DCX):c.305G>A (p.Arg102His)	rs267606317
NM_001195553.2(DCX):c.364+1G>A	rs2147276043
NM_001195553.2(DCX):c.383C>T (p.Ser128Phe)
NM_001195553.2(DCX):c.532C>T (p.Arg178Cys)	rs587783558
NM_001195553.2(DCX):c.533G>T (p.Arg178Leu)	rs587783559
NM_001195553.2(DCX):c.536C>G (p.Pro179Arg)
NM_001195553.2(DCX):c.540G>T (p.Lys180Asn)	rs1927758267
NM_001195553.2(DCX):c.544G>T (p.Val182Phe)	rs1556401951
NM_001195553.2(DCX):c.586C>T (p.Arg196Cys)	rs587783568
NM_001195553.2(DCX):c.596T>C (p.Leu199Pro)	rs587783569
NM_001195553.2(DCX):c.601A>T (p.Lys201Ter)	rs1927748382
NM_001195553.2(DCX):c.667G>C (p.Gly223Arg)	rs587783577
NM_001195553.2(DCX):c.752C>A (p.Ala251Asp)	rs1085307919
NM_001195553.2(DCX):c.757G>C (p.Gly253Arg)	rs1556376311
NM_001195553.2(DCX):c.772C>T (p.Arg258Cys)	rs727503897
NM_001195553.2(DCX):c.799del (p.Asp267fs)	rs2147635206

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