{{Rsnum
|rsid=121913096
|Chromosome=4
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FGG
|position=154606908
|Gene_s=FGG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=134850
|rsnum=121913096
|variant=0019
}}{{ClinVar
|rsid=121913096
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=155528060
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FGG:2266
|GENE_NAME=FGG
|GENE_ID=2266
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.155528060C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000017801.1
|CLNDBN=FIBRINOGEN HILLSBOROUGH
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134850.0019
|Disease=FIBRINOGEN HILLSBOROUGH
}}