{{Rsnum
|rsid=121918220
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VANGL1
|position=115683980
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VANGL1
}}{{omim
|id=610132
|rsnum=121918220
|variant=0003
}}{{ClinVar
|rsid=121918220
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=115683980
|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.115683980T>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_138959.2:c.983T>C; 610132.0003
|CLNSIG=5
|CLNCUI=C0027794
|CLNDBN=Neural tube defect
|Disease=Neural tube defect
|CLNACC=RCV000001413.1
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0027794:182940:ORPHA823:253098009
}}