{{Rsnum
|rsid=2167079
|Gene=ACP2
|Chromosome=11
|position=47248704
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.494
|Gene_s=ACP2,NR1H3
|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 | 10.0 | 41.8 | 48.2
| HCB | 54.0 | 37.2 | 8.8
| JPT | 54.9 | 37.2 | 8.0
| YRI | 40.0 | 42.8 | 17.2
| ASW | 31.6 | 54.4 | 14.0
| CHB | 54.0 | 37.2 | 8.8
| CHD | 60.6 | 31.2 | 8.3
| GIH | 18.8 | 49.5 | 31.7
| LWK | 29.1 | 39.1 | 31.8
| MEX | 15.5 | 39.7 | 44.8
| MKK | 22.2 | 52.9 | 24.8
| TSI | 5.0 | 35.0 | 60.0
| HapMapRevision=28
}}per the [http://blog.23andme.com/2008/12/08/new-papers-from-nature-genetics-yield-a-bounty-of-cholesterol-snps/ 23andMe blog], the minor allele of this SNP (T) was associated with increased [[HDL cholesterol]]
 
{| border="1"
|-
!SNP
!Rarer allele
!LDL
!HDL
!TG
|-
| [[rs6544713]] || T || + || ||
|-
| [[rs2650000]] || A || + || ||
|-
| [[rs471364]] || C || || - ||
|-
| [[rs1800961]] || T || || - ||
|-
| [[rs7679]] || C || || - || +
|-
| [[rs2967605]] || T || || - ||
|-
| [[rs2409722]] || T || || || -
|-
| [[rs10903129]] || A || - || - || -
|-
| [[rs6756629]] || A || - || + || -
|-
| [[rs12670798]] || C || + || + || +
|-
| [[rs7395662]] || A || - || + || +
|-
| [[rs174570]] || T || - || - || +
|-
| [[rs2271293]] || A || - || + || -
|-
| [[rs2624265]] || C || || || +
|-
| [[rs2167079]] || T || || + ||
|-
| [[rs9891572]] || T || || + ||
|-
| [[rs4844614]] || T || + || ||
|-
| [[rs5031002]] || G || + || ||
|-
|}

{{PMID|17357082|OA=1
}} Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.

{{PMID|19060910|OA=1
}} Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.

{{GET Evidence
|gene=ACP2
|aa_change=Arg29Gln
|aa_change_short=R29Q
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2167079
|overall_frequency_n=4076
|overall_frequency_d=10736
|overall_frequency=0.379657
|n_genomes=37
|n_genomes_annotated=0
|n_haplomes=48
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

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