{{Rsnum
|rsid=104894392
|Chromosome=13
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=F10
|position=113149146
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=F10
}}{{omim
|id=227600
|rsnum=104894392
|variant=0001
}}{{ClinVar
|rsid=104894392
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=113803460
|CHROM=13
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=F10:2159
|GENE_NAME=F10
|GENE_ID=2159
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.113803460C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=613872.0001
|CLNSIG=5
|CLNCUI=C0015519
|CLNDBN=Factor X deficiency
|Disease=Factor X deficiency
|CLNACC=RCV000012833.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0015519:227600:328:76642003
}}