{{Rsnum
|rsid=17876030
|Gene=F12
|Chromosome=5
|position=177404825
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=C
|GMAF=0.05372
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=F12
}}{{Venter SNP
|rsid=17876030
|allele=G
|frequency=
|uid=1103654303202
|type=homozygous_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 = 35515200
| distance = 340
}}

{{GET Evidence
|gene=F12
|aa_change=Ala207Pro
|aa_change_short=A207P
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17876030
|overall_frequency_n=10483
|overall_frequency_d=10736
|overall_frequency=0.976434
|n_genomes=55
|n_genomes_annotated=0
|n_haplomes=109
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=2
|autoscore=2
|n_web_uneval=2
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}