{{Rsnum
|rsid=121908121
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=WNT10A
|position=218889990
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WNT10A
}}{{omim
|id=606268
|rsnum=121908121
|variant=0004
}}{{ClinVar
|rsid=121908121
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=219754712
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=WNT10A:80326
|GENE_NAME=WNT10A
|GENE_ID=80326
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.219754712G>A
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=606268.0004; VAR_062510
|CLNSIG=5
|CLNCUI=C0796093
|CLNDBN=Odontoonychodermal dysplasia; Tooth agenesis, selective, 4; not provided
|Disease=Odontoonychodermal dysplasia; Tooth agenesis; not provided
|CLNACC=RCV000004718.1; RCV000030651.1; RCV000059803.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0796093:257980:2721; C1835492:150400:99798
}}{{PMID Auto
|PMID=22581971
|Title=Mutations in WNT10A are present in more than half of isolated hypodontia cases.
}}