{{Rsnum
|rsid=137853262
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OCRL
|position=129567333
|Gene_s=OCRL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300535
|variant=0005
|rsnum=137853262
}}{{ClinVar
|rsid=137853262
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=128701310
|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.128701310A>G
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=300535.0005; VAR_022699
|CLNSIG=5
|CLNCUI=C1845167
|CLNDBN=Dent disease 2
|Disease=Dent disease 2
|CLNACC=RCV000011607.5
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK99494:C1845167:300555:1652:93623
}}{{PMID|15627218|OA=1
}} Dent Disease with mutations in OCRL1.
{{omim
|id=300555
|rsnum=137853262
}}