{{Rsnum
|rsid=3820198
|Gene=LRP8
|Chromosome=1
|position=53326979
|Orientation=minus
|GMAF=0.4789
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=LRP8
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 16.1 | 49.1 | 34.8
| HCB | 19.1 | 47.1 | 33.8
| JPT | 27.4 | 46.9 | 25.7
| YRI | 92.5 | 6.8 | 0.7
| ASW | 70.2 | 24.6 | 5.3
| CHB | 19.1 | 47.1 | 33.8
| CHD | 10.2 | 46.3 | 43.5
| GIH | 26.7 | 50.5 | 22.8
| LWK | 91.8 | 8.2 | 0.0
| MEX | 12.1 | 32.8 | 55.2
| MKK | 79.5 | 19.9 | 0.6
| TSI | 17.6 | 45.1 | 37.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=21316997
|Title=Investigation of LRP8 gene in 1p31 QTL linked to LDL peak particle diameter in the Quebec family study
}}

{{PMID Auto
|PMID=17847002
|Title=An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.
|OA=1
}}

{{GET Evidence
|gene=LRP8
|aa_change=Asp46Glu
|aa_change_short=D46E
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3820198
|overall_frequency_n=5625
|overall_frequency_d=10758
|overall_frequency=0.522867
|n_genomes=44
|n_genomes_annotated=0
|n_haplomes=69
|n_articles=0
|n_articles_annotated=0
|nblosum100=-2
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=22889673
|Title=Association analysis of LRP8 SNP rs3820198 and rs5174 with Parkinson's disease in Han Chinese population.
}}

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