{{Rsnum
|rsid=2227589
|Gene=SERPINC1
|Chromosome=1
|position=173917078
|Orientation=minus
|GMAF=0.1253
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SERPINC1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 1.8 | 16.8 | 81.4
| HCB | 9.5 | 38.0 | 52.6
| JPT | 4.4 | 31.9 | 63.7
| YRI | 0.7 | 11.6 | 87.8
| ASW | 0.0 | 7.0 | 93.0
| CHB | 9.5 | 38.0 | 52.6
| CHD | 11.0 | 48.6 | 40.4
| GIH | 1.0 | 19.8 | 79.2
| LWK | 0.0 | 6.4 | 93.6
| MEX | 0.0 | 5.2 | 94.8
| MKK | 0.0 | 12.2 | 87.8
| TSI | 1.0 | 24.5 | 74.5
| HapMapRevision=28
}}Gene variants associated with [[deep vein thrombosis]].{{PMID|18349091}}

Updated analysis of gene variants associated with [[deep vein thrombosis]].{{PMID|20124536}}

[[rs2227589]] in SERPINC1 (risk allele frequency, 0.10) OR 1.29 (95% CI, 1.10-1.49)

{{PMID|19229049|OA=1
}} associated with plasma anti-FXa activity and antithrombin levels: carriers of the A allele had slightly but significantly lower anticoagulant activity and levels than GG subjects (97.0+/-7.3% vs. 94.6+/-8.4%; p=0.032; 99.5+/-5.8% vs. 94.8+/-5.6%; p=0.001; respectively)

{{PMID Auto
|PMID=20031567
|Title=An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: The Women's Genome Health Study.
|OA=1
}}

{{PMID Auto
|PMID=21232005
|Title=New gene variants associated with venous thrombosis: a replication study in White and Black Americans.
}}

{{PMID Auto
|PMID=23150947
|Title=Single nucleotide polymorphisms and the risk of venous thrombosis: results from a Danish case-cohort study
}}

{{PMID Auto
|PMID=23252292
|Title=[Correlation of coronary heart disease with multiple genes, gene polymorphisms and multiple risk factors in old Chinese Han patients]
}}

{{PMID Auto
|PMID=23954867
|Title=The association of idiopathic recurrent pregnancy loss with polymorphisms in haemostasis-related genes
}}

{{PMID Auto
|PMID=24226152
|Title=Influence of single nucleotide polymorphisms on thrombin generation in factor V Leiden heterozygotes
}}

{{PMID Auto
|PMID=25091233
|Title=Association of F11 polymorphism rs2289252 with deep vein thrombosis and related phenotypes in population of Latvia
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}