{{Rsnum
|rsid=121909607
|Chromosome=4
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FGA
|position=154589513
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGA
}}{{omim
|id=134820
|rsnum=121909607
|variant=0004
}}{{ClinVar
|rsid=121909607
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=155510665
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FGA:2243
|GENE_NAME=FGA
|GENE_ID=2243
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.155510665C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000030941.1
|CLNDBN=Dysfibrinogenemia
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C1260903:111589005
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134820.0004
|Disease=Dysfibrinogenemia
}}