rs3825776
A SNP in the LIPC gene on chromosome 15. Its most notable genotype is C;C: >1.3x increased risk for ALS
- Gene
- LIPC
- Location
- Chr 1558,454,631 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 42%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TGoodNormal risk for ALS
- C;TBad1.3x increased risk for ALS
- C;CMost notableBad>1.3x increased risk for ALS
- A;ANot ratedNo summary available.
SNPedia records rs3825776 on the minus strand: (A;A), (A;G), (G;G), (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 30% C;T 50% C;C 21% A;A 0%
- European ancestry (Utah)T;T 40% C;T 51% C;C 9% A;A 0%
- Han Chinese (Beijing)T;T 30% C;T 50% C;C 20% A;A 0%
- Japanese (Tokyo)T;T 18% C;T 60% C;C 22% A;A 0%
- Yoruba (Nigeria)T;T 26% C;T 59% C;C 16% A;A 0%
- African ancestry (Southwest US)T;T 40% C;T 46% C;C 14% A;A 0%
- Chinese (Denver)T;T 19% C;T 52% C;C 28% A;A 0%
- Gujarati IndianT;T 43% C;T 43% C;C 15% A;A 0%
- Luhya (Kenya)T;T 26% C;T 51% C;C 24% A;A 0%
- Mexican ancestry (Los Angeles)T;T 17% C;T 47% C;C 36% A;A 0%
- Maasai (Kenya)T;T 21% C;T 49% C;C 31% A;A 0%
- TuscanT;T 46% C;T 42% C;C 12% A;A 0%
Related
Other LIPC SNPs
- rs261332A;Aassociated with higher HDL cholesterolWorth 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
rs3825776, a SNP in the region of the LIPC gene on chromosome 15, has been associated with the sporadic form of ALS (Lou Gehrig's disease) in a study of 1000+ European patients. The odds ratio for the risk allele rs3825776(G) is 1.34 (CI: 1.12 - 1.46).
Source and license
Adapted from rs3825776 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.