{{Rsnum
|rsid=118203911
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=F5
|position=169552693
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=F5
}}{{omim
|id=612309
|rsnum=118203911
|variant=0013
}}{{ClinVar
|rsid=118203911
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=169552693
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=F5:2153
|GENE_NAME=F5
|GENE_ID=2153
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.169552693A>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000130.4:c.1160T>C; 612309.0013
|CLNSIG=5
|CLNCUI=C1861171
|CLNDBN=Thrombophilia due to activated protein C resistance
|Disease=Thrombophilia due to activated protein C resistance
|CLNACC=RCV000000689.1
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1368:C1861171:188055
}}