{{Rsnum
|rsid=121965065
|Chromosome=4
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=F11
|position=186285711
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=F11,PRAMEF4
}}{{omim
|id=264900
|rsnum=121965065
|variant=0006
}}{{ClinVar
|rsid=121965065
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=187206865
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=F11-AS1:285441; F11:2160
|GENE_NAME=F11-AS1; F11
|GENE_ID=285441; 2160
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.187206865T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=264900.0006
|CLNSIG=5
|CLNCUI=C0015523
|CLNDBN=Hereditary factor XI deficiency disease
|Disease=Hereditary factor XI deficiency disease
|CLNACC=RCV000012670.20
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0015523:612416:329:49762007
}}