{{Rsnum
|rsid=147210663
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=APOC3
|position=116830844
|Gene_s=APOC3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}[[rs147210663]], also known as A43T, is a rare variant in the apolipoprotein C3 [[APOC3]] gene.

As reported in two large studies published in 2014, [[rs147210663]] is one of several loss of function mutations in the [[APOC3]] gene associated with a >40% lower average triglyceride level in individuals carrying one [[rs147210663]](A) allele and a corresponding decrease in [[coronary artery disease]].{{PMID|24941081}}{{PMID|24941082}}