{{Rsnum
|rsid=80338907
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VLDLR
|position=2643480
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
}}{{omim
|id=192977
|rsnum=80338907
|variant=0002
}}{{ClinVar
|rsid=80338907
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=2643480
|CHROM=9
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=VLDLR:7436
|GENE_NAME=VLDLR
|GENE_ID=7436
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.2643480C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1874; 192977.0002
|CLNSIG=5
|CLNCUI=C0394006
|CLNDBN=Cerebellar ataxia and mental retardation with quadrupedal locomotion 1; Dysequilibrium syndrome
|Disease=Cerebellar ataxia and mental retardation with quadrupedal locomotion 1; Dysequilibrium syndrome
|CLNACC=RCV000012985.21; RCV000020557.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1874:C0394006:224050:1766:230782004
}}{{PMID Auto
|PMID=18326629
|Title=Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans.
|OA=1
}}