{{Rsnum
|rsid=121913105
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=FGFR3
|position=1806163
|Gene_s=FGFR3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=134934
|rsnum=121913105
|variant=0015
}}{{ClinVar
|rsid=121913105
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=1807890
|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.1807890A>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1366; 134934.0015
|CLNSIG=5
|CLNCUI=C2674173; C1868678
|CLNDBN=Achondroplasia, severe, with developmental delay and acanthosis nigricans; Thanatophoric dysplasia type 1
|Disease=Achondroplasia; Thanatophoric dysplasia type 1
|CLNACC=RCV000017749.26; RCV000017750.27
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C2674173; NBK1366:C1868678:187600:2655:85165
}}