{{Rsnum
|rsid=137852521
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=L1CAM
|position=153870933
|Gene_s=L1CAM
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=308840
|variant=0007
|rsnum=137852521
}}{{ClinVar
|rsid=137852521
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=153136388
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=L1CAM:3897
|GENE_NAME=L1CAM
|GENE_ID=3897
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153136388C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=308840.0007
|CLNSIG=5
|CLNCUI=C0265216
|CLNDBN=X-linked hydrocephalus syndrome
|Disease=X-linked hydrocephalus syndrome
|CLNACC=RCV000010672.3
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1484:C0265216:307000:2182:275543:71779008
}}