{{Rsnum
|rsid=118203910
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=F5
|position=169518453
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=F5
}}{{omim
|id=612309
|rsnum=118203910
|variant=0012
}}{{ClinVar
|rsid=118203910
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=169518453
|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.169518453G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000130.4:c.6304C>T; 612309.0012
|CLNSIG=5
|CLNCUI=C0015499
|CLNDBN=Factor V deficiency
|Disease=Factor V deficiency
|CLNACC=RCV000000688.1
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1368:C0015499:227400:ORPHA326:4320005
}}