{{Rsnum
|rsid=104893835
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=WNT7A
|position=13819120
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WNT7A
}}{{omim
|id=601570
|rsnum=104893835
|variant=0001
}}{{ClinVar
|rsid=104893835
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=13860617
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=WNT7A:7476
|GENE_NAME=WNT7A
|GENE_ID=7476
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.13860617G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601570.0001
|CLNSIG=5
|CLNCUI=C1848651
|CLNDBN=Ulna and fibula absence of with severe limb deficiency
|Disease=Ulna and fibula absence of with severe limb deficiency
|CLNACC=RCV000008526.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1848651:276820:2879
}}