{{Rsnum
|rsid=281860301
|Chromosome=11
|position=69818784
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=FGF3
|Gene_s=FGF3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000031938.1
|CLNALLE=1
|CLNDBN=Deafness with labyrinthine aplasia microtia and microdontia (LAMM)
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK100664:C1853144:610706:90024
|CLNHGVS=NC_000011.9:g.69633552G>T
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK100664
|Disease=Deafness with labyrinthine aplasia microtia and microdontia (LAMM)
|FwdALT=A
|FwdREF=C
|REF=G
|RSPOS=69633552
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050360000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=281860301
|GENEINFO=FGF3:2248
|GENE_ID=2248
|GENE_NAME=FGF3
}}