rs2032598

A SNP in the USP9Y gene on chromosome Y. Its most notable genotype is C;C.

Gene
USP9Y
Location
Chr Y12,738,407 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
13%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableNot ratedNo summary available.Typical · 0.032% of people

On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 3 HapMap populations.

  • AverageC;C 32%
  • Han Chinese (Beijing)C;C 0%
  • Japanese (Tokyo)C;C 0%
  • Yoruba (Nigeria)C;C 96%

Other USP9Y SNPs

All USP9Y SNPs

Notes

From SNPedia

Notes

FBXL21 association with schizophrenia in Irish family and case-control samples. MEGF10 association with schizophrenia.

Source and license

Adapted from rs2032598 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.