rs2066715
A SNP in the ABCA1 gene on chromosome 9. Its most notable genotype is C;C: common in complete genomics
- Gene
- ABCA1
- Location
- Chr 9104,825,752 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 13%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2066715 on the minus strand: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 9 HapMap populations.
- AverageC;C 73%
- European ancestry (Utah)C;C 83%
- Han Chinese (Beijing)C;C 30%
- Japanese (Tokyo)C;C 42%
- Yoruba (Nigeria)C;C 99%
- African ancestry (Southwest US)C;C 97%
- Chinese (Denver)C;C 33%
- Gujarati IndianC;C 92%
- Mexican ancestry (Los Angeles)C;C 95%
- TuscanC;C 87%
Related
Other ABCA1 SNPs
- rs4149268C;Tassociated with higher HDL cholesterolWorth knowing
- rs4149274G;GAssociated with higher HDL (good) cholesterol.Minor
- rs363717C;Ccommon in clinvarTypical
- rs2066714T;Tcommon in clinvarTypical
- rs2230808T;Tcommon in clinvarTypical
- rs2297404G;GNo summary available.Typical
- rs2515629A;Acommon in complete genomicsTypical
- rs2853579G;Gcommon in clinvarTypical
Notes
From SNPedia
Notes
Apolipoprotein E levels in cerebrospinal fluid and the effects of ABCA1 polymorphisms. Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review. A survey of ABCA1 sequence variation confirms association with dementia.
Source and license
Adapted from rs2066715 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.