{{Rsnum
|rsid=137853260
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OCRL
|position=129569296
|Gene_s=OCRL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300535
|variant=0003
|rsnum=137853260
}}{{ClinVar
|rsid=137853260
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=128703273
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=OCRL:4952
|GENE_NAME=OCRL
|GENE_ID=4952
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.128703273G>A
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=300535.0003; VAR_010180
|CLNSIG=5
|CLNCUI=C0028860
|CLNDBN=Lowe syndrome
|Disease=Lowe syndrome
|CLNACC=RCV000011605.6
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1480:C0028860:309000:534:79385002
}}{{PMID|9682219}} Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patients.
{{omim
|id=309000
|rsnum=137853260
}}