{{Rsnum
|rsid=121909628
|Chromosome=8
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGFR1
|position=38414892
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR1
}}{{omim
|id=136350
|rsnum=121909628
|variant=0004
}}{{ClinVar
|rsid=121909628
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=38272410
|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.38272410G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=136350.0004
|CLNSIG=255
|CLNCUI=C0271623
|CLNDBN=Kallmann syndrome 2
|Disease=Kallmann syndrome 2
|CLNACC=RCV000030926.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1334:C1563720:147950:478
}}