rs2032597
A SNP in the USP9Y gene on chromosome Y. Its most notable genotype is C;C: M170+
- Gene
- USP9Y
- Location
- Chr Y12,735,858 (GRCh38)
- Highest magnitude
- 1.0Minor
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 4%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (A;C), (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageA;A 93% A;C 0% C;C 7%
- European ancestry (Utah)A;A 71% A;C 0% C;C 29%
- Han Chinese (Beijing)A;A 100% A;C 0% C;C 0%
- Japanese (Tokyo)A;A 100% A;C 0% C;C 0%
- Yoruba (Nigeria)A;A 100% A;C 0% C;C 0%
Related
Other USP9Y SNPs
- rs20320A;ANo summary available.Typical
- rs2032595T;TNo summary available.Typical
- rs2032596T;TNo summary available.Typical
- rs2032598C;CNo summary available.Typical
- rs2032599C;CNo summary available.Typical
- rs2032600C;CNo summary available.Typical
- rs2032601T;TNo summary available.Typical
- rs2032603G;GNo summary available.Typical
Genosets
Genosets combine several genotypes. Twofold checks them in your report.
Notes
From SNPedia
Notes
Also known as M170. The rs2032597(C;C) mutation is a reliable indicator of Haplogroup I (Y-DNA) and is also referred to as M170+. Association of Y chromosome haplogroup I with HIV progression, and HAART outcome.
A;A
M170-
C;C
Match for haplogroup I (Y-DNA).
Source and license
Adapted from rs2032597 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.