{{Rsnum
|rsid=137853261
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=OCRL
|position=129569369
|Gene_s=OCRL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300535
|variant=0004
|rsnum=137853261
}}{{ClinVar
|rsid=137853261
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=128703346
|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.128703346C>G
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=300535.0004; VAR_010184
|CLNSIG=5
|CLNCUI=C0028860
|CLNDBN=Lowe syndrome
|Disease=Lowe syndrome
|CLNACC=RCV000011606.9
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1480:C0028860:309000:534:79385002
}}{{PMID|9632163}} Oculocerebrorenal syndrome of Lowe: three mutations in the OCRL1 gene derived from three patients with different phenotypes.
{{omim
|id=309000
|rsnum=137853261
}}