rs15285
A SNP in the LPL gene on chromosome 8. Its most notable genotype is C;C: common in clinvar
- Gene
- LPL
- Location
- Chr 819,967,156 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 33%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs15285 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 11 HapMap populations.
- AverageC;C 45%
- European ancestry (Utah)C;C 54%
- Han Chinese (Beijing)C;C 66%
- Japanese (Tokyo)C;C 66%
- Yoruba (Nigeria)C;C 17%
- African ancestry (Southwest US)C;C 19%
- Chinese (Denver)C;C 62%
- Gujarati IndianC;C 62%
- Luhya (Kenya)C;C 22%
- Mexican ancestry (Los Angeles)C;C 52%
- Maasai (Kenya)C;C 24%
- TuscanC;C 46%
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 rs15285 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.