{{Rsnum
|rsid=2000999
|Gene=HPR
|Chromosome=16
|position=72074194
|Orientation=plus
|GMAF=0.197
|Gene_s=HPR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 3.7 | 25.7 | 70.6
| HCB | 13.2 | 33.1 | 53.7
| JPT | 13.5 | 45.9 | 40.5
| YRI | 0.7 | 8.9 | 90.4
| ASW | 1.8 | 8.8 | 89.5
| CHB | 13.2 | 33.1 | 53.7
| CHD | 7.5 | 46.2 | 46.2
| GIH | 23.5 | 46.9 | 29.6
| LWK | 1.9 | 19.4 | 78.7
| MEX | 3.6 | 32.1 | 64.3
| MKK | 0.0 | 9.4 | 90.6
| TSI | 5.9 | 36.6 | 57.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20686565
|Trait=None
|Title=Biological, clinical and population relevance of 95 loci for blood lipids.
|RiskAllele=A
|Pval=2E-22
|OR=2.0000
|ORtxt=None
|OA=1
}}
{{PMID Auto GWAS
|PMID=22403646
|Trait=None
|Title=A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels.
|RiskAllele=A
|Pval=8E-59
|OR=0.1380
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=22579477
|Title=Clinical necessity of partitioning of human plasma haptoglobin reference intervals by recently-discovered rs2000999.
}}

{{PMID Auto
|PMID=20066028
|Title=Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels.
|OA=1
}}

{{PMID Auto
|PMID=22433445
|Title=Complexity of a complex trait locus: HP, HPR, haemoglobin and cholesterol.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}