{{Rsnum
|rsid=281860307
|Chromosome=11
|position=69810567
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TG)
|geno3=(TG;TG)
|Gene=FGF3
|Gene_s=FGF3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=C
|CHROM=11
|CLNACC=RCV000022694.24
|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.69625335_69625336delCA
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK100664; 164950.0009
|Disease=Deafness with labyrinthine aplasia microtia and microdontia (LAMM)
|FwdREF=TG
|REF=CCA
|RSPOS=69625334
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050360000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=281860307
|GENEINFO=FGF3:2248
|GENE_ID=2248
|GENE_NAME=FGF3
}}