{{Rsnum
|rsid=121909637
|Chromosome=8
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FGFR1
|position=38418249
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR1
}}{{omim
|id=136350
|rsnum=121909637
|variant=0016
}}{{ClinVar
|rsid=121909637
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=38275767
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FGFR1:2260
|GENE_NAME=FGFR1
|GENE_ID=2260
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.38275767C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=136350.0016
|CLNSIG=255
|CLNCUI=C0271623
|CLNDBN=Kallmann syndrome 2
|Disease=Kallmann syndrome 2
|CLNACC=RCV000030932.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1334:C1563720:147950:478
}}