rs2697962(C;C)

Normal risk of developing Parkinson's Disease

Magnitude
1.0Minor
Repute
Good
Frequency
68%Average of 11 populations
On SNPedia
rs2697962(G;G)Minus strand
Gene
PRDM2

Frequency

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

  • African ancestry (Southwest US)80%
  • Yoruba (Nigeria)78%
  • European ancestry (Utah)74%
  • Luhya (Kenya)74%
  • Maasai (Kenya)72%
  • Tuscan71%
  • Han Chinese (Beijing)69%
  • Chinese (Denver)66%
  • Mexican ancestry (Los Angeles)65%
  • Japanese (Tokyo)52%
  • Gujarati Indian43%

Other genotypes of rs2697962

  1. T;TMost notableBadIncreased risk of developing Parkinson's DiseaseWorth knowing · 2.03% of people
  2. C;TBadSlightly increased risk of developing Parkinson's DiseaseMinor · 1.529% of people
  3. G;GNot ratedNo summary available.Typical · 0.00% of people

All about rs2697962

Source and license

Adapted from rs2697962(G;G) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.