{{Rsnum
|rsid=121917705
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FGF3
|position=69818738
|Gene_s=FGF3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=164950
|rsnum=121917705
|variant=0004
}}{{ClinVar
|rsid=121917705
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=69633506
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=FGF3:2248
|GENE_NAME=FGF3
|GENE_ID=2248
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.69633506C>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK100664; 164950.0004
|CLNSIG=5
|CLNCUI=C1853144
|CLNDBN=Deafness with labyrinthine aplasia microtia and microdontia (LAMM)
|Disease=Deafness with labyrinthine aplasia microtia and microdontia (LAMM)
|CLNACC=RCV000014852.24
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK100664:C1853144:610706:90024
}}