{{Rsnum
|rsid=121918218
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=VANGL1
|position=115664171
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VANGL1
}}{{omim
|id=610132
|rsnum=121918218
|variant=0001
}}{{ClinVar
|rsid=121918218
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=115664171
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=VANGL1:81839
|GENE_NAME=VANGL1
|GENE_ID=81839
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.115664171G>A
|CLNORIGIN=0
|CLNSIG=5
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000001411.1
|CLNDBN=Caudal regression syndrome
|CLNDSDB=MedGen
|CLNDSDBID=C0300948
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_138959.2:c.715G>A; 610132.0001
|Disease=Caudal regression syndrome
}}