{{Rsnum
|rsid=80338753
|Chromosome=2
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TTTG)
|geno3=(TTTG;TTTG)
|Gene=LRP2
|position=169169727
|Gene_s=LRP2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80338753
|Reversed=1
|FwdREF=TTTG
|FwdALT=
|REF=CCAAA
|ALT=C
|RSPOS=170026236
|CHROM=2
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110200
|GENEINFO=LRP2:4036
|GENE_NAME=LRP2
|GENE_ID=4036
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.170026237_170026240delCAAA
|CLNSRC=GeneReviews
|CLNORIGIN=0
|CLNSRCID=NBK1878
|CLNSIG=5
|CLNCUI=C1857277
|CLNDBN=Donnai Barrow syndrome
|Disease=Donnai Barrow syndrome
|CLNACC=RCV000020603.1
|Tags=RV;PM;PMC;S3D;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
}}