{{Rsnum
|rsid=3813948
|Gene=C4BPB
|Chromosome=1
|position=207096513
|Orientation=minus
|GMAF=0.1166
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=C4BPB
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 79.5 | 19.6 | 0.9
| HCB | 66.9 | 31.6 | 1.5
| JPT | 74.3 | 22.1 | 3.5
| YRI | 61.9 | 38.1 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 66.9 | 31.6 | 1.5
| CHD | 0.0 | 0.0 | 0.0
| GIH | 78.2 | 20.8 | 1.0
| LWK | 67.3 | 29.1 | 3.6
| MEX | 84.2 | 14.0 | 1.8
| MKK | 0.0 | 0.0 | 0.0
| TSI | 82.5 | 16.5 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20212171
|Trait=Plasma C4b binding protein levels
|Title=C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies
|RiskAllele=C
|Pval=4E-10
|OR=None
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}