{{Rsnum
|rsid = 28933068
|Gene = FGFR3
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=G
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Chromosome=4
|position=1805644
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR3
}}{{omim
|desc=HYPOCHONDROPLASIA
|id=134934
|rsnum=28933068
|variant=0010
}}
{{ neighbor
| rsid = 28928869
| distance = 515
}}

{{ClinVar
|rsid=28933068
|Reversed=0
|FwdREF=C
|FwdALT=A,G
|REF=C
|ALT=A,G
|RSPOS=1807371
|CHROM=4
|dbSNPBuildID=131
|SSR=0
|SAO=0
|VP=0x050260000000000402110100
|GENEINFO=FGFR3:2261
|GENE_NAME=FGFR3
|GENE_ID=2261
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000004.11:g.1807371C>A; NC_000004.11:g.1807371C>G
|CLNSRC=GTR; GeneReviews; OMIM Allelic Variant
|CLNSRCID=GTR000509343; NBK1477; 134934.0010; 134934.0034; GTR000500509; 134934.0012
|CLNSIG=5
|CLNCUI=C0410529
|CLNDBN=Hypochondroplasia; Thanatophoric dysplasia type 1
|Disease=Hypochondroplasia; Thanatophoric dysplasia type 1
|CLNACC=RCV000017740.27; RCV000017771.22; RCV000017741.27
|Tags=PM;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1477:C0410529:146000:429:205468002; NBK1366:C1868678:187600:2655:85165
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}