{{Rsnum
|rsid=121909625
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGB
|position=154565832
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGB
}}{{omim
|id=134830
|rsnum=121909625
|variant=0016
}}{{ClinVar
|rsid=121909625
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=155486984
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FGB:2244
|GENE_NAME=FGB
|GENE_ID=2244
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.155486984C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000017822.26
|CLNDBN=Hypofibrinogenemia, congenital
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134830.0016
|Disease=Hypofibrinogenemia
}}