{{Rsnum
|rsid=121913075
|Chromosome=1
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=F13B
|position=197055720
|Gene_s=F13B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=134580
|rsnum=121913075
|variant=0002
}}{{ClinVar
|rsid=121913075
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=197055720
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=F13B:2165
|GENE_NAME=F13B
|GENE_ID=2165
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.197055720C>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001994.2:c.1349G>T; 134580.0002
|CLNSIG=5
|CLNCUI=C2750481
|CLNDBN=Factor xiii, b subunit, deficiency of
|Disease=Factor xiii
|CLNACC=RCV000017983.26
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2750481:613235:ORPHA331
}}