{{Rsnum
|rsid=80358305
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LRP5
|position=68348188
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LRP5
}}{{omim
|id=603506
|rsnum=80358305
|variant=0025
}}{{ClinVar
|rsid=80358305
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=68115656
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=LRP5:4041
|GENE_NAME=LRP5
|GENE_ID=4041
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.68115656C>T
|CLNORIGIN=0
|CLNSIG=5
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000006672.1; RCV000033256.2
|CLNDBN=Exudative vitreoretinopathy 4, autosomal dominant; Osteoporosis with pseudoglioma
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0432252:259770:2788:254112001
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603506.0025
|Disease=Exudative vitreoretinopathy 4; Osteoporosis with pseudoglioma
}}{{PMID Auto
|PMID=15981244
|Title=Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes.
}}