{{Rsnum
|rsid=6415084
|Gene=LPA
|Chromosome=6
|position=160559298
|Orientation=plus
|GMAF=0.3329
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=LPA
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 29.2 | 49.6 | 21.2
| HCB | 83.2 | 15.3 | 1.5
| JPT | 78.6 | 21.4 | 0.0
| YRI | 40.8 | 43.5 | 15.6
| ASW | 38.6 | 45.6 | 15.8
| CHB | 83.2 | 15.3 | 1.5
| CHD | 81.7 | 17.4 | 0.9
| GIH | 56.4 | 39.6 | 4.0
| LWK | 38.2 | 50.0 | 11.8
| MEX | 41.4 | 43.1 | 15.5
| MKK | 42.9 | 39.7 | 17.3
| TSI | 22.5 | 55.9 | 21.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=20160194
|Title=Comprehensive analysis of genomic variation in the LPA locus and its relationship to plasma lipoprotein(a) in South Asians, Chinese, and European Caucasians
}}

{{PMID Auto
|PMID=21283670
|Title=Single-nucleotide polymorphisms in LPA explain most of the ancestry-specific variation in Lp(a) levels in African Americans.
|OA=1
}}

{{PMID Auto
|PMID=23230442
|Title=Association study of lipoprotein(a) genetic markers, traditional risk factors, and coronary heart disease in HIV-1-infected patients
|OA=1
}}

{{PMID Auto
|PMID=23978127
|Title=Lack of association between lipoprotein(a) genetic variants and subsequent cardiovascular events in Chinese Han patients with coronary artery disease after percutaneous coronary intervention
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}