{{Rsnum
|rsid=104893886
|Chromosome=5
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FGF10
|position=44305155
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGF10
}}{{omim
|id=602115
|rsnum=104893886
|variant=0004
}}{{ClinVar
|rsid=104893886
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=44305257
|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.44305257A>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000007967.1
|CLNDBN=Ladd syndrome
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602115.0004
|Disease=Ladd syndrome
}}