{{Rsnum
|rsid=121909621
|Chromosome=4
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FGB
|position=154569703
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGB
}}{{omim
|id=134830
|rsnum=121909621
|variant=0009
}}{{ClinVar
|rsid=121909621
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=155490855
|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.155490855T>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000017815.26
|CLNDBN=Afibrinogenemia, congenital
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134830.0009
|Disease=Afibrinogenemia
}}