{{Rsnum
|rsid=118203906
|Gene=F5
|Chromosome=1
|position=169555299
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=F5
}}{{omim
|id=612309
|rsnum=118203906
|variant=0003
}}{{ClinVar
|rsid=118203906
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=169555299
|CHROM=1
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000a05000016110100
|GENEINFO=F5:2153
|GENE_NAME=F5
|GENE_ID=2153
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.169555299C>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000130.4:c.1001G>C; 612309.0003
|CLNSIG=5
|CLNCUI=C1861171
|CLNDBN=Thrombophilia due to activated protein C resistance
|Disease=Thrombophilia due to activated protein C resistance
|CLNACC=RCV000000678.1
|Tags=RV;PM;NSM;REF;ASP;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1368:C1861171:188055
|COMMON=0
}}