{{Rsnum
|rsid=318240760
|Chromosome=10
|position=120871178
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=WDR11
|Gene_s=WDR11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=A
|CHROM=10
|CLNACC=RCV000030849.1; RCV000059797.1
|CLNALLE=1
|CLNDBN=Hypogonadotropic hypogonadism 14 with or without anosmia; not provided
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN158713:614858:478
|CLNHGVS=NC_000010.10:g.122630690G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=606417.0002; VAR_069195
|Disease=Hypogonadotropic hypogonadism 14 with or without anosmia; not provided
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=122630690
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050168000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=318240760
|GENEINFO=WDR11:55717
|GENE_ID=55717
|GENE_NAME=WDR11
}}{{PMID Auto
|PMID=20887964
|Title=WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
|OA=1
}}