{{Rsnum
|rsid=267607168
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VANGL2
|position=160425122
|Gene_s=VANGL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=1
|CLNACC=RCV000009620.1
|CLNALLE=1
|CLNDBN=Neural tube defect
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0027794:182940:ORPHA823:253098009
|CLNHGVS=NC_000001.11:g.160425122T>C
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_020335.2:c.1310T>C; 600533.0002
|Disease=Neural tube defect
|FwdALT=C
|FwdREF=T
|GENEINFO=VANGL2:57216
|GENE_ID=57216
|GENE_NAME=VANGL2
|REF=T
|RSPOS=160425122
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=267607168
|CLNORIGIN=1
}}