{{Rsnum
|rsid=80338752
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LRP2
|position=169178001
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LRP2
}}{{omim
|id=600073
|rsnum=80338752
|variant=0006
}}{{ClinVar
|rsid=80338752
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=170034511
|CHROM=2
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=LRP2:4036
|GENE_NAME=LRP2
|GENE_ID=4036
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.170034511G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1878; 600073.0006
|CLNSIG=5
|CLNCUI=C1857277; C1857277
|CLNDBN=Donnai Barrow syndrome
|Disease=Donnai Barrow syndrome
|CLNACC=RCV000010063.3
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1878:C1857277:222448:2143
}}{{PMID Auto
|PMID=8266995
|Title=Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?
}}

{{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
}}