rs261332
A SNP in the LIPC gene on chromosome 15. Its most notable genotype is A;A: associated with higher HDL cholesterol
- Gene
- LIPC
- Location
- Chr 1558,435,126 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 19%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableGoodassociated with higher HDL cholesterol
- A;GGoodassociated with higher HDL cholesterol
- G;GGoodcommon in complete genomics
On SNPedia: (A;A), (A;G), (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.
- AverageA;A 4% A;G 30% G;G 66%
- European ancestry (Utah)A;A 6% A;G 35% G;G 59%
- Han Chinese (Beijing)A;A 4% A;G 23% G;G 73%
- Japanese (Tokyo)A;A 7% A;G 51% G;G 42%
- Yoruba (Nigeria)A;A 5% A;G 38% G;G 57%
- African ancestry (Southwest US)A;A 5% A;G 35% G;G 60%
- Chinese (Denver)A;A <1% A;G 20% G;G 79%
- Gujarati IndianA;A 4% A;G 28% G;G 68%
- Luhya (Kenya)A;A 4% A;G 29% G;G 67%
- Mexican ancestry (Los Angeles)A;A 7% A;G 16% G;G 77%
- Maasai (Kenya)A;A 2% A;G 26% G;G 72%
- TuscanA;A 3% A;G 25% G;G 72%
Related
Conditions, medicines and genes
Other LIPC SNPs
- rs3825776C;C>1.3x increased risk for ALSWorth knowing
- rs6083A;Acommon in clinvarTypical
- rs261334C;Ccommon in complete genomicsTypical
- rs261342C;Ccommon in complete genomicsTypical
- rs2070895G;Gcommon in complete genomicsTypical
- rs3829462C;Ccommon in clinvarTypical
- rs8023503C;Ccommon in complete genomicsTypical
- rs12594375G;Gcommon in complete genomicsTypical
Notes
From SNPedia
Notes
rs261332 increases susceptibility to Elevated HDL-Cholesterol for carriers of the A allele A allele is associated with 1.41mg/dl increase in HDL cholesterol (good cholesterol).
Source and license
Adapted from rs261332 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.