{{Rsnum
|rsid = 28928868
|Gene = FGFR3
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=4
|position=1806164
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR3
}}{{omim
|desc=HYPOCHONDROPLASIA
|id=134934
|rsnum=28928868
|variant=0020
}}
{{ neighbor
| rsid = 28928869
| distance = 5
}}

{{ClinVar
|rsid=28928868
|Reversed=0
|FwdREF=G
|FwdALT=C,T
|REF=G
|ALT=C,T
|RSPOS=1807891
|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.1807891G>C; NC_000004.11:g.1807891G>T
|CLNSRC=OMIM Allelic Variant; GeneReviews
|CLNSRCID=134934.0021; NBK1477; 134934.0020
|CLNSIG=5
|CLNCUI=C0410529
|CLNDBN=Hypochondroplasia
|Disease=Hypochondroplasia
|CLNACC=RCV000017756.26; RCV000017755.27
|Tags=PM;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1477:C0410529:146000:429:205468002
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}