{{Rsnum
|rsid=121918480
|Chromosome=11
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=F2
|position=46739341
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=F2
}}{{omim
|id=176930
|rsnum=121918480
|variant=0005
}}{{ClinVar
|rsid=121918480
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=46760891
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=F2:2147
|GENE_NAME=F2
|GENE_ID=2147
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.46760891G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176930.0005
|CLNSIG=5
|CLNCUI=C0272317
|CLNDBN=Hereditary factor II deficiency disease
|Disease=Hereditary factor II deficiency disease
|CLNACC=RCV000014233.22
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0272317:33297000
}}