{{Rsnum
|rsid=387906484
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=OCRL
|position=129589905
|Gene_s=OCRL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=X
|CLNACC=RCV000011604.5
|CLNALLE=1
|CLNDBN=Lowe syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1480:C0028860:309000:534:79385002
|CLNHGVS=NC_000023.10:g.128723882C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300535.0002
|Disease=Lowe syndrome
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=128723882
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906484
|GENEINFO=OCRL:4952
|GENE_ID=4952
|GENE_NAME=OCRL
}}