rs10513789(T;T)

Very common. Normal risk of Parkinson's disease.

Magnitude
1.3Minor
Repute
Not rated
Frequency
47%Average of 11 populations
On SNPedia
rs10513789(T;T)
Gene
MCCC1

Frequency

Share of people with T;T in each HapMap population.

  • Luhya (Kenya)74%
  • Yoruba (Nigeria)69%
  • African ancestry (Southwest US)64%
  • Tuscan64%
  • Maasai (Kenya)59%
  • European ancestry (Utah)56%
  • Mexican ancestry (Los Angeles)41%
  • Gujarati Indian39%
  • Japanese (Tokyo)17%
  • Han Chinese (Beijing)16%
  • Chinese (Denver)16%

Other genotypes of rs10513789

  1. G;GMost notableGood0.64x decreased risk of Parkinson's diseaseMinor · 1.812% of people
  2. G;TGood0.8x decreased risk of Parkinson's diseaseMinor · 1.441% of people

All about rs10513789

Notes

From SNPedia

Approximately 55% of non-asian people have this genotype which is associated with slightly higher risk of Parkinson's disease when compared to genotype (G;G). It is notable because it is the first SNP patented by 23andMe rs10513789(T) increased risk of developing Parkinson's Disease GenomicsLawReport

Source and license

Adapted from rs10513789(T;T) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.