{{Rsnum
|rsid=121918219
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=VANGL1
|position=115682372
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VANGL1
}}{{omim
|id=610132
|rsnum=121918219
|variant=0002
}}{{ClinVar
|rsid=121918219
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=115682372
|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.115682372G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_138959.2:c.821G>A; 610132.0002
|CLNSIG=5
|CLNCUI=C0027794
|CLNDBN=Neural tube defect
|Disease=Neural tube defect
|CLNACC=RCV000001412.1
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0027794:182940:ORPHA823:253098009
}}