{{Rsnum
|rsid=80053154
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGFR3
|position=1805636
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR3
}}{{omim
|id=134934
|rsnum=80053154
|variant=0019
}}{{ClinVar
|rsid=80053154
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=1807363
|CHROM=4
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050260000000000402110100
|GENEINFO=FGFR3:2261
|GENE_NAME=FGFR3
|GENE_ID=2261
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.1807363A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1477; 134934.0019
|CLNSIG=5
|CLNCUI=C0410529
|CLNDBN=Hypochondroplasia
|Disease=Hypochondroplasia
|CLNACC=RCV000017754.27
|Tags=RV;PM;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1477:C0410529:146000:429:205468002
}}