{{Rsnum
|rsid=121908652
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=WNT4
|position=22129682
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WNT4
}}{{omim
|id=603490
|rsnum=121908652
|variant=0003
}}{{ClinVar
|rsid=121908652
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=22129682
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=WNT4:54361
|GENE_NAME=WNT4
|GENE_ID=54361
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.22129682G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_030761.4:c.247C>T; 603490.0003
|CLNSIG=5
|CLNCUI=C2675014
|CLNDBN=Mullerian aplasia and hyperandrogenism
|Disease=Mullerian aplasia and hyperandrogenism
|CLNACC=RCV000006690.1
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2675014:158330:ORPHA3109
}}