{{Rsnum
|rsid=199988476
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=F12
|position=177402460
|Gene_s=F12,PFN3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=5
|CLNACC=RCV000001225.2
|CLNALLE=1
|CLNDBN=Factor XII deficiency disease
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0015526:234000:46981006
|CLNHGVS=NC_000005.9:g.176829461C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=610619.0003
|Disease=Factor XII deficiency disease
|FwdALT=T
|FwdREF=C
|GENEINFO=F12:2161; PFN3:345456
|GENE_ID=2161; 345456
|GENE_NAME=F12; PFN3
|REF=C
|RSPOS=176829461
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=199988476
}}