{{Rsnum
|rsid=78311289
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FGFR3
|position=1806162
|Gene_s=FGFR3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=134934
|variant=0004
|rsnum=78311289
}}{{ClinVar
|rsid=78311289
|Reversed=0
|FwdREF=A
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=1807889
|CHROM=4
|dbSNPBuildID=131
|SSR=0
|SAO=3
|VP=0x050260000000000402110120
|GENEINFO=FGFR3:2261
|GENE_NAME=FGFR3
|GENE_ID=2261
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000004.11:g.1807889A>C; NC_000004.11:g.1807889A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1477; 134934.0022; NBK1366; 134934.0004
|CLNSIG=255
|CLNCUI=C0410529; C1300257
|CLNDBN=Hypochondroplasia; Thanatophoric dysplasia, type 2; Multiple myeloma, somatic; Spermatocytic seminoma, somatic
|Disease=Hypochondroplasia; Thanatophoric dysplasia; Multiple myeloma; Spermatocytic seminoma
|CLNACC=RCV000017757.27; RCV000017728.23; RCV000017729.1; RCV000017730.1
|Tags=PM;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1477:C0410529:146000:429:205468002; NBK1366:C1300257:187601:2655:93274:389158007
}}