{{Rsnum
|rsid=2923084
|Chromosome=11
|position=10367235
|Orientation=plus
|GMAF=0.3618
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CAND1.11
|Gene_s=CAND1.11
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 72.6 | 23.9 | 3.5
| HCB | 25.0 | 52.2 | 22.8
| JPT | 21.2 | 43.4 | 35.4
| YRI | 21.2 | 57.5 | 21.2
| ASW | 29.8 | 47.4 | 22.8
| CHB | 25.0 | 52.2 | 22.8
| CHD | 22.9 | 38.5 | 38.5
| GIH | 75.2 | 22.8 | 2.0
| LWK | 22.7 | 60.0 | 17.3
| MEX | 32.8 | 55.2 | 12.1
| MKK | 51.3 | 42.3 | 6.4
| TSI | 71.6 | 25.5 | 2.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20686565
|Trait=None
|Title=Biological, clinical and population relevance of 95 loci for blood lipids.
|RiskAllele=G
|Pval=5E-8
|OR=0.4100
|ORtxt=None
|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 | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}