{{Rsnum
|rsid=17610395
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CPT1A
|position=68794860
|Status=Merged
|Merged=2229738
|Gene_s=CPT1A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 17.0 | 83.0
| HCB | 0.0 | 0.8 | 99.2
| JPT | 0.0 | 1.8 | 98.2
| YRI | 0.0 | 0.7 | 99.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.8 | 99.2
| CHD | 0.0 | 0.9 | 99.1
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 2.7 | 97.3
| MEX | 0.0 | 8.6 | 91.4
| MKK | 0.0 | 0.0 | 0.0
| TSI | 1.0 | 11.8 | 87.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22286219
|Trait=None
|Title=Genome-wide association study identifies multiple loci influencing human serum metabolite levels.
|RiskAllele=
|Pval=8E-12
|OR=0.1700
|ORtxt=None
|OA=1
}}

{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}