rs118204059
A SNP in the LPL gene on chromosome 8. Its most notable genotype is A;A: Hyperlipoproteinemia, type I
- Gene
- LPL
- Location
- Chr 819,955,876 (GRCh38)
- Highest magnitude
- 4.0Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBadHyperlipoproteinemia, type I
- A;TBadCarrier for Hyperlipoproteinemia, type I
- T;TGoodcommon in clinvar
On SNPedia: (A;A), (A;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other LPL SNPs
- rs118204057A;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
- rs15285C;Ccommon in clinvarTypical
Source and license
Adapted from rs118204059 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.