rs1059611
A SNP in the LPL gene on chromosome 8. Its most notable genotype is T;T: common in clinvar
- Gene
- LPL
- Location
- Chr 819,967,052 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 12%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (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.
- AverageT;T 77%
- European ancestry (Utah)T;T 79%
- Han Chinese (Beijing)T;T 82%
- Japanese (Tokyo)T;T 82%
- Yoruba (Nigeria)T;T 66%
- African ancestry (Southwest US)T;T 68%
- Chinese (Denver)T;T 77%
- Gujarati IndianT;T 78%
- Luhya (Kenya)T;T 70%
- Mexican ancestry (Los Angeles)T;T 88%
- Maasai (Kenya)T;T 76%
- TuscanT;T 79%
Related
Other LPL SNPs
- rs118204057A;AHyperlipoproteinemia, type IVery important
- rs118204059A;AHyperlipoproteinemia, type IVery important
- rs118204060T;THyperlipoproteinemia, type IVery important
- rs268G;G3X+ increased risk for venous thromboembolismWorth knowing
- rs326A;Alower HDL cholesterolWorth knowing
- rs321G;Gcommon in complete genomicsTypical
- rs325T;TNo summary available.Typical
- rs328C;Ccommon in clinvarTypical
Source and license
Adapted from rs1059611 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.