{{Rsnum
|rsid=121908670
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LRP5
|position=68363784
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LRP5
}}{{omim
|id=603506
|rsnum=121908670
|variant=0015
}}{{ClinVar
|rsid=121908670
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=68131252
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=LRP5:4041
|GENE_NAME=LRP5
|GENE_ID=4041
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.68131252G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603506.0015
|CLNSIG=5
|CLNCUI=C0432273; C1843330; C1843323
|CLNDBN=Worth disease; Osteopetrosis autosomal dominant type 1; Van Buchem disease type 2
|Disease=Worth disease; Osteopetrosis autosomal dominant type 1; Van Buchem disease type 2
|CLNACC=RCV000006660.1; RCV000006661.1; RCV000006662.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT; MedGen:OMIM:Orphanet; MedGen:OMIM
|CLNDSDBID=C0432273:144750:254131007; C1843330:607634:2783; C1843323:607636
}}