{{Rsnum
|rsid=104893887
|Chromosome=5
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=FGF10
|position=44310447
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGF10
}}{{omim
|id=602115
|rsnum=104893887
|variant=0005
}}{{ClinVar
|rsid=104893887
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=44310549
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FGF10:2255
|GENE_NAME=FGF10
|GENE_ID=2255
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.44310549T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602115.0005
|CLNSIG=5
|CLNCUI=C0158667
|CLNDBN=Congenital absence of salivary gland; Ladd syndrome
|Disease=Congenital absence of salivary gland; Ladd syndrome
|CLNACC=RCV000007968.1; RCV000007969.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0158667:180920:22589009
}}