{{Rsnum
|rsid=121918486
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=F2
|position=46739324
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=F2
}}{{omim
|id=176930
|rsnum=121918486
|variant=0013
}}{{ClinVar
|rsid=121918486
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=46760874
|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.46760874C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176930.0013
|CLNSIG=5
|CLNCUI=C0272317
|CLNDBN=Hereditary factor II deficiency disease
|Disease=Hereditary factor II deficiency disease
|CLNACC=RCV000014242.16
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0272317:33297000
}}