{{Rsnum
|rsid=80358321
|Chromosome=11
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=LRP5
|position=68438453
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LRP5
}}{{omim
|id=603506
|rsnum=80358321
|variant=0021
}}{{ClinVar
|rsid=80358321
|Reversed=0
|FwdREF=ACA
|FwdALT=C
|REF=A
|ALT=AC
|RSPOS=68205919
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.68205921_68205922insC
|CLNORIGIN=0
|CLNSIG=5
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000006668.1
|CLNDBN=Exudative vitreoretinopathy 4, autosomal dominant
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603506.0021
|Disease=Exudative vitreoretinopathy 4
|GENEINFO=LRP5:4041
|GENE_ID=4041
|GENE_NAME=LRP5
}}{{PMID Auto
|PMID=15024691
|Title=Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.
|OA=1
}}