{{Rsnum
|rsid=137852660
|Gene=FGF8
|Chromosome=10
|position=101775209
|Orientation=minus
|GMAF=0.0004591
|Gene_s=FGF8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{omim
|id=600483
|variant=0002
|rsnum=137852660
}}{{ClinVar
|rsid=137852660
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=103534966
|CHROM=10
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|GENEINFO=FGF8:2253
|GENE_NAME=FGF8
|GENE_ID=2253
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.103534966G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600483.0002
|CLNSIG=5
|CLNCUI=C2675188
|CLNDBN=Kallmann syndrome 6
|Disease=Kallmann syndrome 6
|CLNACC=RCV000009692.1
|Tags=RV;PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1334:C2675188:612702:478
|COMMON=0
}}