rs287235

A SNP in the USP24 gene on chromosome 1. Its most notable genotype is C;G.

Gene
USP24
Location
Chr 155,212,826 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, FamilyTreeDNA
Minor allele frequency
26%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;GMost notableNot ratedNo summary available.Typical · 0.034% of people

On SNPedia: (C;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.

  • AverageC;G 34%
  • European ancestry (Utah)C;G 37%
  • Han Chinese (Beijing)C;G 22%
  • Japanese (Tokyo)C;G 12%
  • Yoruba (Nigeria)C;G 44%
  • African ancestry (Southwest US)C;G 58%
  • Chinese (Denver)C;G 20%
  • Gujarati IndianC;G 27%
  • Luhya (Kenya)C;G 46%
  • Mexican ancestry (Los Angeles)C;G 19%
  • Maasai (Kenya)C;G 46%
  • TuscanC;G 41%

Conditions, medicines and genes

Other USP24 SNPs

All USP24 SNPs

Notes

From SNPedia

Notes

The (G) allele of this snp has been implicated in a somewhat increased risk of developing late onset Parkinson's disease

C;G

PMID 16917932 This genotype appears to have increased risk for late-onset Parkinson's disease

References

Source and license

Adapted from rs287235 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.