{{Rsnum
|rsid=121909634
|Chromosome=8
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGFR1
|position=38419676
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR1
}}{{omim
|id=136350
|rsnum=121909634
|variant=0012
}}{{ClinVar
|rsid=121909634
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=38277194
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FGFR1:2260
|GENE_NAME=FGFR1
|GENE_ID=2260
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.38277194A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=136350.0012
|CLNSIG=5
|CLNCUI=C0432283
|CLNDBN=Osteoglophonic dysplasia
|Disease=Osteoglophonic dysplasia
|CLNACC=RCV000017682.22
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0432283:166250:254144002
}}