{{Rsnum
|rsid=137852522
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=L1CAM
|position=153862856
|Gene_s=L1CAM
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=308840
|variant=0009
|rsnum=137852522
}}{{ClinVar
|rsid=137852522
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=153128311
|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.153128311G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=308840.0009
|CLNSIG=5
|CLNCUI=C0265216; C0795953
|CLNDBN=X-linked hydrocephalus syndrome; Spastic paraplegia 1
|Disease=X-linked hydrocephalus syndrome; Spastic paraplegia 1
|CLNACC=RCV000010674.2; RCV000010675.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1484:C0265216:307000:2182:275543:71779008; NBK1484:C0795953:303350:2466:275543
}}