{{Rsnum
|rsid=61753266
|Gene=F10
|Chromosome=13
|position=113140972
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=F10
}}{{omim
|id=227600
|rsnum=61753266
|variant=0007
}}{{ClinVar
|rsid=61753266
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=113795286
|CHROM=13
|GMAF=0.0009
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050060000000040016110100
|GENEINFO=F10:2159
|GENE_NAME=F10
|GENE_ID=2159
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.113795286G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=613872.0007
|CLNSIG=5
|CLNCUI=C0015519
|CLNDBN=Factor X deficiency
|Disease=Factor X deficiency
|CLNACC=RCV000012841.1
|Tags=PM;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0015519:227600:328:76642003
|COMMON=0
}}