rs10501570

A SNP in the DLG2 gene on chromosome 11. Its most notable genotype is T;T: Normal risk of developing Parkinson's Disease

Gene
DLG2
Location
Chr 1184,706,803 (GRCh38)
Highest magnitude
1.0Minor
Tested on
23andMe, AncestryDNA
Minor allele frequency
10%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodNormal risk of developing Parkinson's DiseaseMinor · 1.086% of people

On SNPedia: (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 86%
  • European ancestry (Utah)T;T 63%
  • Han Chinese (Beijing)T;T 96%
  • Japanese (Tokyo)T;T 97%
  • Yoruba (Nigeria)T;T 100%
  • African ancestry (Southwest US)T;T 97%
  • Chinese (Denver)T;T 95%
  • Gujarati IndianT;T 76%
  • Luhya (Kenya)T;T 98%
  • Mexican ancestry (Los Angeles)T;T 62%
  • Maasai (Kenya)T;T 94%
  • TuscanT;T 62%

Other DLG2 SNPs

All DLG2 SNPs

Notes

From SNPedia

Notes

Detecting disease-associated genotype patterns. Phactr2 and Parkinson's disease.

Source and license

Adapted from rs10501570 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.