{{Rsnum
|rsid=137852525
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=L1CAM
|position=153866826
|Gene_s=L1CAM
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=308840
|variant=0014
|rsnum=137852525
}}{{ClinVar
|rsid=137852525
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=153132281
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=L1CAM:3897
|GENE_NAME=L1CAM
|GENE_ID=3897
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153132281C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000010680.3
|CLNDBN=HYDROCEPHALUS, X-LINKED, WITH HIRSCHSPRUNG DISEASE
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=308840.0014
|Disease=HYDROCEPHALUS
}}