{{Rsnum
|rsid=77722678
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGFR3
|position=1805643
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR3
}}{{omim
|id=134934
|rsnum=77722678
|variant=0023
}}{{ClinVar
|rsid=77722678
|Reversed=1
|FwdREF=T
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=1807370
|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; 2
|CLNHGVS=NC_000004.11:g.1807370A>C; NC_000004.11:g.1807370A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1477; 134934.0018; 134934.0023
|CLNSIG=5
|CLNCUI=C0410529
|CLNDBN=Hypochondroplasia
|Disease=Hypochondroplasia
|CLNACC=RCV000017753.27; RCV000017758.27
|Tags=RV;PM;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1477:C0410529:146000:429:205468002
}}