{{Rsnum
|rsid = 28939709
|Gene = LRP5
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=11
|position=68436987
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LRP5
}}{{omim
|desc=EXUDATIVE VITREORETINOPATHY 4, AUTOSOMAL RECESSIVE
|id=603506
|rsnum=28939709
|variant=0024
}}{{ClinVar
|rsid=28939709
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=68204455
|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.68204455G>A
|CLNORIGIN=0
|CLNSIG=5
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000006671.1
|CLNDBN=Exudative vitreoretinopathy 4, autosomal recessive
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603506.0024
|Disease=Exudative vitreoretinopathy 4
}}{{PMID|15346351|OA=1
}} Autosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5.

{{on chip | 23andMe v4}}