{{Rsnum
|rsid=629301
|Gene=CELSR2
|Chromosome=1
|position=109275684
|Orientation=minus
|GMAF=0.2135
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=CELSR2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 54.9 | 38.1 | 7.1
| HCB | 92.0 | 8.0 | 0.0
| JPT | 84.1 | 14.2 | 1.8
| YRI | 44.2 | 50.3 | 5.4
| ASW | 26.3 | 61.4 | 12.3
| CHB | 92.0 | 8.0 | 0.0
| CHD | 92.7 | 6.4 | 0.9
| GIH | 56.4 | 33.7 | 9.9
| LWK | 19.1 | 57.3 | 23.6
| MEX | 70.7 | 24.1 | 5.2
| MKK | 44.9 | 46.2 | 9.0
| TSI | 61.8 | 31.4 | 6.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20686565
|Trait=None
|Title=Biological, clinical and population relevance of 95 loci for blood lipids
|RiskAllele=G
|Pval=0
|OR=5.65
|ORtxt=[NR] unit decrease
|OA=1
}}

{{omim
|id=613589
|rsnum=629301
}}

{{PMID Auto
|PMID=18262040
|Title=LDL-cholesterol concentrations: a genome-wide association study.
|OA=1
}}

{{PMID Auto
|PMID=19913121
|Title=Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
|OA=1
}}

{{PMID Auto
|PMID=20502693
|Title=Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.
|OA=1
}}

{{PMID Auto
|PMID=23092954
|Title=SHAVE: shrinkage estimator measured for multiple visits increases power in GWAS of quantitative traits.
|OA=1
}}

{{PMID Auto
|PMID=23723249
|Title=GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications.
|OA=1
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}