{{Rsnum
|rsid=118203912
|Chromosome=1
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=F5
|position=169560701
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=F5
}}{{omim
|id=612309
|rsnum=118203912
|variant=0014
}}{{ClinVar
|rsid=118203912
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=169560701
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000605000002110100
|GENEINFO=F5:2153
|GENE_NAME=F5
|GENE_ID=2153
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.169560701C>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000130.4:c.439G>T; 612309.0014
|CLNSIG=5
|CLNCUI=C1861171
|CLNDBN=Thrombophilia due to activated protein C resistance
|Disease=Thrombophilia due to activated protein C resistance
|CLNACC=RCV000000679.1
|Tags=RV;PM;S3D;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1368:C1861171:188055
}}