{{Rsnum
|rsid=1436958
|Gene=VPS13C
|Chromosome=15
|position=62046598
|Orientation=plus
|GMAF=0.3641
|Gene_s=VPS13C
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 31.9 | 51.3 | 16.8
| HCB | 42.2 | 47.4 | 10.4
| JPT | 37.2 | 48.7 | 14.2
| YRI | 68.7 | 26.5 | 4.8
| ASW | 70.2 | 26.3 | 3.5
| CHB | 42.2 | 47.4 | 10.4
| CHD | 49.1 | 38.0 | 13.0
| GIH | 44.6 | 36.6 | 18.8
| LWK | 77.6 | 19.6 | 2.8
| MEX | 17.2 | 48.3 | 34.5
| MKK | 58.3 | 36.5 | 5.1
| TSI | 45.0 | 41.0 | 14.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23382691
  |Trait=IgG glycosylation
  |Title=Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
  |RiskAllele=G
  |Pval=9E-6
  |OR=.14
  |ORtxt=[0.078-0.2] unit increase
  |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 | Illumina Human 1M}}