{{Rsnum
|rsid=121908119
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=WNT10A
|position=218882368
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WNT10A
}}{{omim
|id=606268
|rsnum=121908119
|variant=0002
}}{{ClinVar
|rsid=121908119
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=219747090
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000040002110100
|GENEINFO=WNT10A:80326
|GENE_NAME=WNT10A
|GENE_ID=80326
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.219747090C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606268.0002
|CLNSIG=5
|CLNCUI=C0796093; C1857069
|CLNDBN=Odontoonychodermal dysplasia; Schopf-Schulz-Passarge syndrome; Tooth agenesis, selective, 4
|Disease=Odontoonychodermal dysplasia; Schopf-Schulz-Passarge syndrome; Tooth agenesis
|CLNACC=RCV000004715.1; RCV000004716.1; RCV000030650.1
|Tags=PM;VLD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0796093:257980:2721; C1857069:224750:50944; C1835492:150400:99798
}}