{{Rsnum
|rsid=11933531
|Gene=CCSER1
|Chromosome=4
|position=91494378
|Orientation=plus
|GMAF=0.1281
|Gene_s=CCSER1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 13.3 | 86.7
| HCB | 7.3 | 37.2 | 55.5
| JPT | 6.2 | 44.2 | 49.6
| YRI | 0.0 | 17.7 | 82.3
| ASW | 0.0 | 8.8 | 91.2
| CHB | 7.3 | 37.2 | 55.5
| CHD | 7.3 | 44.0 | 48.6
| GIH | 5.9 | 34.7 | 59.4
| LWK | 0.9 | 11.8 | 87.3
| MEX | 1.7 | 36.2 | 62.1
| MKK | 1.3 | 21.2 | 77.6
| TSI | 1.0 | 5.9 | 93.1
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23725790
  |Trait=DNA methylation (variation)
  |Title=GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
  |RiskAllele=A
  |Pval=3E-8
  |OR=NR
  |ORtxt=NR
  }}

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