{{Rsnum
|rsid=10935120
|Gene=CEP63
|Chromosome=3
|position=134514250
|Orientation=plus
|GMAF=0.3196
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CEP63
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 7.1 | 46.0 | 46.9
| HCB | 1.5 | 30.7 | 67.9
| JPT | 5.3 | 34.5 | 60.2
| YRI | 27.2 | 52.4 | 20.4
| ASW | 14.0 | 57.9 | 28.1
| CHB | 1.5 | 30.7 | 67.9
| CHD | 2.8 | 28.7 | 68.5
| GIH | 14.9 | 47.5 | 37.6
| LWK | 40.9 | 40.9 | 18.2
| MEX | 0.0 | 34.5 | 65.5
| MKK | 12.8 | 50.0 | 37.2
| TSI | 13.7 | 43.1 | 43.1
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=18391952
|Trait=Height
|Title=Genome-wide association analysis identifies 20 loci that influence adult height
|RiskAllele=A
|Pval=7.0000000000000005E-8
|OR=0.06
|ORtxt=[0.03-0.09] SD shorter - among males
|OA=1
}}

{{PMID Auto
|PMID=19030899
|Title=Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.
|OA=1
}}

{{PMID Auto
|PMID=19557189
|Title=Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.
|OA=1
}}

{{PMID Auto
|PMID=20017971
|Title=Assessing the impact of global versus local ancestry in association studies.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10935120
|overall_frequency_n=65
|overall_frequency_d=128
|overall_frequency=0.507812
|n_genomes=41
|n_genomes_annotated=0
|n_haplomes=56
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}