rs4922115
A SNP in the LPL gene on chromosome 8. Its most notable genotype is G;G: common in clinvar
- Gene
- LPL
- Location
- Chr 819,965,319 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (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.
- AverageG;G 80%
- European ancestry (Utah)G;G 74%
- Han Chinese (Beijing)G;G 87%
- Japanese (Tokyo)G;G 82%
- Yoruba (Nigeria)G;G 85%
- African ancestry (Southwest US)G;G 77%
- Chinese (Denver)G;G 82%
- Gujarati IndianG;G 88%
- Luhya (Kenya)G;G 85%
- Mexican ancestry (Los Angeles)G;G 69%
- Maasai (Kenya)G;G 73%
- TuscanG;G 75%
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 rs4922115 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.