{{Rsnum
|rsid=80338743
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LRP2
|position=169290999
|Gene_s=LRP2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80338743
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=170147509
|CHROM=2
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=LRP2:4036
|GENE_NAME=LRP2
|GENE_ID=4036
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.170147509T>C
|CLNSRC=GeneReviews
|CLNORIGIN=0
|CLNSRCID=NBK1878
|CLNSIG=5
|CLNCUI=C1857277
|CLNDBN=Donnai Barrow syndrome
|Disease=Donnai Barrow syndrome
|CLNACC=RCV000020605.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1878:C1857277:222448:2143
}}{{PMID Auto
|PMID=17632512
|Title=Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes.
|OA=1
}}