{{Rsnum
|rsid=12328675
|Gene=COBLL1
|Chromosome=2
|position=164684290
|Orientation=plus
|GMAF=0.1152
|Gene_s=COBLL1
|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 | 0.9 | 27.7 | 71.4
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 4.8 | 34.0 | 61.2
| ASW | 0.0 | 33.3 | 66.7
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 1.0 | 17.8 | 81.2
| LWK | 6.4 | 30.9 | 62.7
| MEX | 0.0 | 19.0 | 81.0
| MKK | 3.8 | 17.3 | 78.8
| TSI | 2.9 | 31.4 | 65.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20686565
|Trait=None
|Title=Biological, clinical and population relevance of 95 loci for blood lipids.
|RiskAllele=C
|Pval=3E-10
|OR=0.6800
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=23160641
|Title=Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes.
|OA=1
}}

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