{{Rsnum
|rsid=1007190
|Gene=C1QL1
|Chromosome=17
|position=44960841
|Orientation=plus
|GMAF=0.1492
|Gene_s=C1QL1
|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 | 81.4 | 18.6 | 0.0
| HCB | 64.2 | 32.1 | 3.6
| JPT | 64.6 | 29.2 | 6.2
| YRI | 73.5 | 24.5 | 2.0
| ASW | 77.2 | 22.8 | 0.0
| CHB | 64.2 | 32.1 | 3.6
| CHD | 72.5 | 23.9 | 3.7
| GIH | 83.2 | 14.9 | 2.0
| LWK | 67.9 | 29.4 | 2.8
| MEX | 60.3 | 36.2 | 3.4
| MKK | 69.2 | 28.2 | 2.6
| TSI | 86.3 | 12.7 | 1.0
| 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=T
  |Pval=2E-6
  |OR=NR
  |ORtxt=NR
  }}

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