{{Rsnum
|rsid=4635554
|Chromosome=2
|position=21166787
|Orientation=plus
|GMAF=0.393
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 14.5 | 40.3 | 45.2
| HCB | 11.9 | 66.7 | 21.4
| JPT | 23.3 | 34.9 | 41.9
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 11.9 | 66.7 | 21.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20657596
|Trait=Hypertriglyceridemia
|Title=Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
|RiskAllele=G
|Pval=2E-7
|OR=1.67
|ORtxt=[1.38-2.02]
|OA=1
}}