rs10468017

A SNP in the LOC101928635 gene on chromosome 15. Its most notable genotype is C;T: associated with higher HDL cholesterol

Gene
LOC101928635
Location
Chr 1558,386,313 (GRCh38)
Highest magnitude
2.0Worth knowing
Tested on
23andMe, AncestryDNA
Minor allele frequency
21%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;TMost notableGoodassociated with higher HDL cholesterolWorth knowing · 2.029% of people
  2. T;TGoodassociated with higher HDL cholesterolWorth knowing · 2.04% of people

On SNPedia: (C;T), (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.

  • AverageC;T 29% T;T 4%
  • European ancestry (Utah)C;T 53% T;T 5%
  • Han Chinese (Beijing)C;T 28% T;T 5%
  • Japanese (Tokyo)C;T 36% T;T 5%
  • Yoruba (Nigeria)C;T 18% T;T 1%
  • African ancestry (Southwest US)C;T 20% T;T 5%
  • Chinese (Denver)C;T 23% T;T 3%
  • Gujarati IndianC;T 31% T;T 6%
  • Luhya (Kenya)C;T 16% T;T <1%
  • Mexican ancestry (Los Angeles)C;T 28% T;T 2%
  • Maasai (Kenya)C;T 29% T;T 3%
  • TuscanC;T 36% T;T 6%

Conditions, medicines and genes

Notes

From SNPedia

Notes

T allele is associated with 1.76mg/dl increase in HDL cholesterol (good cholesterol).

Source and license

Adapted from rs10468017 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.