{{Rsnum
|rsid=121913482
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGFR3
|position=1801837
|Gene_s=FGFR3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=134934
|rsnum=121913482
|variant=0005
}}{{ClinVar
|rsid=121913482
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=1803564
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=3
|VP=0x050060000000000002110120
|GENEINFO=FGFR3:2261
|GENE_NAME=FGFR3
|GENE_ID=2261
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.1803564C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=2
|CLNSRCID=NBK1366; 134934.0005
|CLNSIG=255
|CLNCUI=C1868678
|CLNDBN=Thanatophoric dysplasia type 1; Multiple myeloma, somatic; Skeletal dysplasia with acanthosis nigricans; Nevus, epidermal, somatic; Keratosis, seborrheic, somatic
|Disease=Thanatophoric dysplasia type 1; Multiple myeloma; Skeletal dysplasia with acanthosis nigricans; Nevus; Keratosis
|CLNACC=RCV000017731.27; RCV000017732.1; RCV000017733.26; RCV000017734.1; RCV000017735.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1366:C1868678:187600:2655:85165
}}