{{Rsnum
|rsid=104894779
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=DCX
|position=111410215
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DCX
}}{{omim
|id=300121
|rsnum=104894779
|variant=0001
}}{{ClinVar
|rsid=104894779
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=110653443
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=DCX:1641
|GENE_NAME=DCX
|GENE_ID=1641
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.110653443C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300121.0001
|CLNSIG=5
|CLNCUI=C1848199
|CLNDBN=X-linked lissencephaly; Subcortical laminar heterotopia, X-linked
|Disease=X-linked lissencephaly; Subcortical laminar heterotopia
|CLNACC=RCV000012355.15; RCV000012356.23
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1185:C1848199:300067:2148; C1848070
}}