{{Rsnum
|rsid=121909606
|Chromosome=4
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGA
|position=154589514
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGA
}}{{omim
|id=134820
|rsnum=121909606
|variant=0003
}}{{ClinVar
|rsid=121909606
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=155510666
|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.155510666G>A
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000017825.1; RCV000017840.1
|CLNDBN=Dysfibrinogenemia; Fibrinogen milano xii, digenic
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C1260903:111589005
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134820.0003; 134820.0022
|Disease=Dysfibrinogenemia; Fibrinogen milano xii
}}