{{Rsnum
|rsid=387906522
|Chromosome=11
|position=46723421
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=F2
|Gene_s=F2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=GT
|CHROM=11
|CLNACC=RCV000014236.16
|CLNALLE=1
|CLNDBN=Prothrombin deficiency, congenital
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0020640:613679:325:73975000
|CLNHGVS=NC_000011.9:g.46744971_46744972insT
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=176930.0008
|Disease=Prothrombin deficiency
|FwdALT=T
|REF=G
|RSPOS=46744971
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906522
|GENEINFO=F2:2147
|GENE_ID=2147
|GENE_NAME=F2
}}