{{Rsnum
|rsid=121913066
|Chromosome=6
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=F13A1
|position=6182121
|Gene_s=F13A1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=134570
|rsnum=121913066
|variant=0004
}}{{ClinVar
|rsid=121913066
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=6182354
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=F13A1:2162
|GENE_NAME=F13A1
|GENE_ID=2162
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.6182354G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=134570.0004
|CLNSIG=5
|CLNCUI=C2750514
|CLNDBN=Factor xiii, a subunit, deficiency of
|Disease=Factor xiii
|CLNACC=RCV000017990.22
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2750514:613225:331
}}