{{Rsnum
|rsid=104893832
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=WNT7A
|position=13854777
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WNT7A
}}{{omim
|id=601570
|rsnum=104893832
|variant=0002
}}{{ClinVar
|rsid=104893832
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=13896274
|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.13896274C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601570.0002
|CLNSIG=5
|CLNCUI=C1856728
|CLNDBN=Fuhrmann syndrome
|Disease=Fuhrmann syndrome
|CLNACC=RCV000008527.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1856728:228930:2854
}}