{{Rsnum
|rsid=104893884
|Gene=FGF10
|Chromosome=5
|position=44305045
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=FGF10
}}{{omim
|id=602115
|rsnum=104893884
|variant=0001
}}{{ClinVar
|rsid=104893884
|Reversed=1
|FwdREF=C
|FwdALT=G,T
|REF=G
|ALT=A,C
|RSPOS=44305147
|CHROM=5
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000016110100
|GENEINFO=FGF10:2255
|GENE_NAME=FGF10
|GENE_ID=2255
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.44305147G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602115.0001
|CLNSIG=5
|CLNCUI=C0158667
|CLNDBN=Congenital absence of salivary gland
|Disease=Congenital absence of salivary gland
|CLNACC=RCV000007964.2
|Tags=RV;PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0158667:180920:22589009
|COMMON=0
}}