{{Rsnum
|rsid=104894785
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=DCX
|position=111410134
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DCX
}}{{omim
|id=300121
|rsnum=104894785
|variant=0012
}}{{ClinVar
|rsid=104894785
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=110653362
|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.110653362G>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000012372.15
|CLNDBN=Subcortical laminar heterotopia, X-linked
|CLNDSDB=MedGen
|CLNDSDBID=C1848070
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300121.0012
|Disease=Subcortical laminar heterotopia
}}