{{Rsnum
|rsid=7604827
|Gene=VWC2L
|Chromosome=2
|position=214477166
|Orientation=plus
|GMAF=0.1488
|Gene_s=VWC2L
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 19.5 | 80.5
| HCB | 0.0 | 3.6 | 96.4
| JPT | 0.0 | 1.8 | 98.2
| YRI | 14.3 | 49.0 | 36.7
| ASW | 12.3 | 43.9 | 43.9
| CHB | 0.0 | 3.6 | 96.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 1.0 | 12.9 | 86.1
| LWK | 13.6 | 45.5 | 40.9
| MEX | 0.0 | 27.6 | 72.4
| MKK | 14.1 | 47.4 | 38.5
| TSI | 1.0 | 25.5 | 73.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23534349
  |Trait=PR interval
  |Title=Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.
  |RiskAllele=C
  |Pval=5E-6
  |OR=6.54
  |ORtxt=[NR] ms increase
  }}

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