rs6083
A SNP in the LIPC gene on chromosome 15. Its most notable genotype is A;A: common in clinvar
- Gene
- LIPC
- Location
- Chr 1558,545,811 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 41%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (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 16% G;G 44%
- European ancestry (Utah)A;A 44% G;G 15%
- Han Chinese (Beijing)A;A 4% G;G 63%
- Japanese (Tokyo)A;A 0% G;G 89%
- Yoruba (Nigeria)A;A 8% G;G 46%
- African ancestry (Southwest US)A;A 7% G;G 51%
- Chinese (Denver)A;A 3% G;G 64%
- Gujarati IndianA;A 25% G;G 30%
- Luhya (Kenya)A;A 7% G;G 44%
- Mexican ancestry (Los Angeles)A;A 19% G;G 28%
- Maasai (Kenya)A;A 10% G;G 45%
- TuscanA;A 48% G;G 5%
Related
Other LIPC SNPs
- rs261332A;Aassociated with higher HDL cholesterolWorth knowing
- rs3825776C;C>1.3x increased risk for ALSWorth knowing
- 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
Source and license
Adapted from rs6083 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.