{{Rsnum
|rsid=137852664
|Chromosome=10
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGF8
|position=101770378
|Gene_s=FGF8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600483
|variant=0006
|rsnum=137852664
}}{{ClinVar
|rsid=137852664
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=103530135
|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.103530135G>A
|CLNORIGIN=1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000009697.1
|CLNDBN=Reclassified - variant of unknown significance
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600483.0006
|Disease=Reclassified - variant of unknown significance
}}