{{Rsnum
|rsid=137852661
|Chromosome=10
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGF8
|position=101775168
|Gene_s=FGF8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600483
|variant=0003
|rsnum=137852661
}}{{ClinVar
|rsid=137852661
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=103534925
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FGF8:2253
|GENE_NAME=FGF8
|GENE_ID=2253
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.103534925A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600483.0003
|CLNSIG=5
|CLNCUI=C0271623
|CLNDBN=Kallmann syndrome 6
|Disease=Kallmann syndrome 6
|CLNACC=RCV000030887.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1334:C2675188:612702:478
}}