{{Rsnum
|rsid=3733860
|Gene=SV2C
|Chromosome=5
|position=76326989
|Orientation=plus
|GMAF=0.1896
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=SV2C
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.9 | 19.5 | 79.6
| HCB | 14.2 | 47.8 | 38.1
| JPT | 27.0 | 39.6 | 33.3
| YRI | 0.0 | 0.7 | 99.3
| ASW | 0.0 | 1.8 | 98.2
| CHB | 14.2 | 47.8 | 38.1
| CHD | 17.9 | 46.2 | 35.8
| GIH | 0.0 | 24.8 | 75.2
| LWK | 0.0 | 0.9 | 99.1
| MEX | 10.3 | 32.8 | 56.9
| MKK | 0.0 | 3.9 | 96.1
| TSI | 1.0 | 18.8 | 80.2
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23650146
  |Trait=Venous thromboembolism
  |Title=A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
  |RiskAllele=A
  |Pval=8E-6
  |OR=1.19
  |ORtxt=[1.10-1.29]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}