{{Rsnum
|rsid=121965070
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=F11
|position=186280065
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=F11
}}{{omim
|id=264900
|rsnum=121965070
|variant=0013
}}{{ClinVar
|rsid=121965070
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=187201219
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000040002110100
|GENEINFO=F11:2160
|GENE_NAME=F11
|GENE_ID=2160
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.187201219A>T
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=264900.0013; VAR_054900
|CLNSIG=5
|CLNCUI=C0015523
|CLNDBN=Hereditary factor XI deficiency disease; not provided
|Disease=Hereditary factor XI deficiency disease; not provided
|CLNACC=RCV000012677.21; RCV000059034.1
|Tags=PM;PMC;S3D;SLO;VLD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0015523:612416:329:49762007
}}{{PMID Auto
|PMID=15180874
|Title=Severe factor XI deficiency caused by compound heterozygosity.
}}