{{Rsnum
|rsid=2217332
|Gene=HERPUD1
|Chromosome=16
|position=56935236
|Orientation=plus
|GMAF=0.1166
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=HERPUD1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 77.9 | 21.2 | 0.9
| HCB | 81.8 | 18.2 | 0.0
| JPT | 89.4 | 10.6 | 0.0
| YRI | 74.8 | 25.2 | 0.0
| ASW | 78.9 | 21.1 | 0.0
| CHB | 81.8 | 18.2 | 0.0
| CHD | 81.7 | 17.4 | 0.9
| GIH | 68.3 | 29.7 | 2.0
| LWK | 82.7 | 16.4 | 0.9
| MEX | 63.8 | 34.5 | 1.7
| MKK | 83.3 | 16.7 | 0.0
| TSI | 72.5 | 23.5 | 3.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20694148
|Trait=None
|Title=A genome-wide association study of the metabolic syndrome in Indian Asian men
|RiskAllele=
|Pval=0.000003
|OR=None
|ORtxt=None
|OA=1
}}

{{PMID|20031564|OA=1
}} Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study.

{{GET Evidence
|gene=HERPUD1
|aa_change=Arg50His
|aa_change_short=R50H
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2217332
|overall_frequency_n=1609
|overall_frequency_d=10758
|overall_frequency=0.149563
|n_genomes=19
|n_genomes_annotated=0
|n_haplomes=19
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.003
|nblosum100=1
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}