{{Rsnum
|rsid=35515200
|Gene=F12
|Chromosome=5
|position=177405165
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=G
|GMAF=0.002755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=F12
}}{{Venter SNP
|rsid=35515200
|allele=C
|frequency=
|uid=1103654303190
|type=heterozygous_SNP
|hugo=F12
|ensembl gene=ENSG00000131187
|ensembl transcript=ENST00000253496
|sift=TOLERATED
|disease=Defects in F12 do not cause any clinical symptoms. The sole effect is that whole-blood clotting time is prolonged.
}}
{{ neighbor
| rsid = 17876030
| distance = 340
}}

{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}