rs2066714
A SNP in the ABCA1 gene on chromosome 9. Its most notable genotype is T;T: common in clinvar
- Gene
- ABCA1
- Location
- Chr 9104,824,472 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
- Minor allele frequency
- 37%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2066714 on the minus strand: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageT;T 37%
- European ancestry (Utah)T;T 74%
- Han Chinese (Beijing)T;T 6%
- Japanese (Tokyo)T;T 21%
- Yoruba (Nigeria)T;T 20%
- African ancestry (Southwest US)T;T 26%
- Chinese (Denver)T;T 9%
- Gujarati IndianT;T 74%
- Luhya (Kenya)T;T 20%
- Mexican ancestry (Los Angeles)T;T 56%
- Maasai (Kenya)T;T 33%
- TuscanT;T 71%
Related
Other ABCA1 SNPs
- rs4149268C;Tassociated with higher HDL cholesterolWorth knowing
- rs4149274G;GAssociated with higher HDL (good) cholesterol.Minor
- rs363717C;Ccommon in clinvarTypical
- rs2066715C;Ccommon in complete genomicsTypical
- 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. Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery. Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review. Association of genetic variants with chronic kidney disease in Japanese individuals. A survey of ABCA1 sequence variation confirms association with dementia.
Source and license
Adapted from rs2066714 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.