{{Rsnum
|rsid=2066715
|Gene=ABCA1
|Chromosome=9
|position=104825752
|Orientation=minus
|GMAF=0.1281
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ABCA1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 16.8 | 83.2
| HCB | 13.9 | 56.2 | 29.9
| JPT | 11.5 | 46.9 | 41.6
| YRI | 0.0 | 0.7 | 99.3
| ASW | 0.0 | 3.5 | 96.5
| CHB | 13.9 | 56.2 | 29.9
| CHD | 14.8 | 51.9 | 33.3
| GIH | 1.0 | 6.9 | 92.1
| LWK | 0.0 | 0.0 | 0.0
| MEX | 1.7 | 3.4 | 94.8
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 12.7 | 87.3
| HapMapRevision=28
}}

{{PMID Auto
|PMID=21247457
|Title=Genetic variant of V825I in the ATP-binding cassette transporter A1 gene and serum lipid levels in the Guangxi Bai Ku Yao and Han populations
|OA=1
}}

{{PMID|17430597|OA=1
}} Apolipoprotein E levels in cerebrospinal fluid and the effects of ABCA1 polymorphisms.

{{PMID|19041386|OA=1
}} Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.

{{PMID|19606474|OA=1
}} A survey of ABCA1 sequence variation confirms association with dementia.

{{GET Evidence
|gene=ABCA1
|aa_change=Val825Ile
|aa_change_short=V825I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2066715
|overall_frequency_n=512
|overall_frequency_d=10758
|overall_frequency=0.0475925
|n_genomes=7
|n_genomes_annotated=0
|n_haplomes=9
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=-4
|autoscore=3
|n_web_uneval=10
}}

{{PMID Auto
|PMID=23355348
|Title=Interactions of several single nucleotide polymorphisms and high body mass index on serum lipid traits.
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}