rs17482753
A SNP on chromosome 8. Its most notable genotype is G;G: normal
- Gene
- None listed
- Location
- Chr 819,975,135 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 9%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G), (G;T), (T;T). 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.
- AverageG;G 85% G;T 14% T;T <1%
- European ancestry (Utah)G;G 81% G;T 16% T;T 3%
- Han Chinese (Beijing)G;G 81% G;T 18% T;T <1%
- Japanese (Tokyo)G;G 81% G;T 18% T;T <1%
- Yoruba (Nigeria)G;G 91% G;T 9% T;T 0%
- African ancestry (Southwest US)G;G 86% G;T 12% T;T 2%
- Chinese (Denver)G;G 77% G;T 22% T;T <1%
- Gujarati IndianG;G 82% G;T 18% T;T 0%
- Luhya (Kenya)G;G 95% G;T 5% T;T <1%
- Mexican ancestry (Los Angeles)G;G 88% G;T 12% T;T 0%
- Maasai (Kenya)G;G 92% G;T 8% T;T 0%
- TuscanG;G 79% G;T 18% T;T 3%
Notes
From SNPedia
Notes
rs17482753 increases susceptibility to Elevated HDL-Cholesterol for carriers of the T allele rs17482753 increases susceptibility to Elevated triglycerides for carriers of the T allele
Source and license
Adapted from rs17482753 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.