{{Rsnum
|rsid=121965063
|Chromosome=4
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=F11
|position=186274193
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=F11
}}{{omim
|id=264900
|rsnum=121965063
|variant=0002
}}{{ClinVar
|rsid=121965063
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=187195347
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040002110100
|GENEINFO=F11:2160
|GENE_NAME=F11
|GENE_ID=2160
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.187195347G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=264900.0002
|CLNSIG=5
|CLNCUI=C0015523
|CLNDBN=Hereditary factor XI deficiency disease
|Disease=Hereditary factor XI deficiency disease
|CLNACC=RCV000012666.21
|Tags=PM;S3D;VLD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0015523:612416:329:49762007
}}