{{Rsnum
|rsid = 4647924
|Gene = FGFR3
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=G
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Chromosome=4
|position=1801844
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR3
}}{{omim
|desc=MUENKE SYNDROME
|id=134934
|rsnum=4647924
|variant=0014
}}

{{ClinVar
|rsid=4647924
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=1803571
|CHROM=4
|dbSNPBuildID=111
|SSR=0
|SAO=1
|VP=0x050060000000000502110100
|GENEINFO=FGFR3:2261
|GENE_NAME=FGFR3
|GENE_ID=2261
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.1803571C>G
|CLNSRC=GTR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=GTR000206858; 134934.0014
|CLNSIG=5
|CLNCUI=C1864436; C0175699
|CLNDBN=Muenke syndrome; Saethre-Chotzen syndrome; Beare-Stevenson syndrome-like anomalies
|Disease=Muenke syndrome; Saethre-Chotzen syndrome; Beare-Stevenson syndrome-like anomalies
|CLNACC=RCV000017746.28; RCV000017747.22; RCV000017748.26
|Tags=PM;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1415:NBK1455:C1864436:602849:53271:440350001; NBK1189:C0175699:101400:794:83015004
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}