{{Rsnum
|rsid=121913113
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FGFR3
|position=1806076
|Gene_s=FGFR3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=134934
|rsnum=121913113
|variant=0029
}}{{ClinVar
|rsid=121913113
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=1807803
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FGFR3:2261
|GENE_NAME=FGFR3
|GENE_ID=2261
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.1807803G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=134934.0029
|CLNSIG=5
|CLNCUI=C1864852
|CLNDBN=Camptodactyly, tall stature, and hearing loss syndrome
|Disease=Camptodactyly
|CLNACC=RCV000017765.26
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1864852:610474:85164
}}