{{Rsnum
|rsid=80358322
|Chromosome=11
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=LRP5
|position=68439918
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LRP5
}}{{omim
|id=603506
|rsnum=80358322
|variant=0020
}}{{ClinVar
|rsid=80358322
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=68207386
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=LRP5:4041
|GENE_NAME=LRP5
|GENE_ID=4041
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.68207386T>G
|CLNORIGIN=0
|CLNSIG=5
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000006667.1
|CLNDBN=Exudative vitreoretinopathy 4, autosomal dominant
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603506.0020
|Disease=Exudative vitreoretinopathy 4
}}{{PMID Auto
|PMID=15024691
|Title=Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.
|OA=1
}}