{{Rsnum
|rsid=121918349
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=WNT10B
|position=48966271
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WNT10B
}}{{omim
|id=601906
|rsnum=121918349
|variant=0001
}}{{ClinVar
|rsid=121918349
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=49360054
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=WNT10B:7480
|GENE_NAME=WNT10B
|GENE_ID=7480
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.49360054G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601906.0001
|CLNSIG=5
|CLNCUI=C2749665
|CLNDBN=Split-hand/foot malformation 6
|Disease=Split-hand/foot malformation 6
|CLNACC=RCV000008069.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2749665:225300:2440
}}