{{Rsnum
|rsid=121917703
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGF3
|position=69810559
|Gene_s=FGF3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=164950
|rsnum=121917703
|variant=0001
}}{{ClinVar
|rsid=121917703
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=69625327
|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.69625327A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK100664; 164950.0001
|CLNSIG=5
|CLNCUI=C1853144
|CLNDBN=Deafness with labyrinthine aplasia microtia and microdontia (LAMM)
|Disease=Deafness with labyrinthine aplasia microtia and microdontia (LAMM)
|CLNACC=RCV000014849.24
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK100664:C1853144:610706:90024
}}