rs2032631
A SNP in the KDM5D gene on chromosome Y. Its most notable genotype is A;A.
- Gene
- KDM5D
- Location
- Chr Y19,705,901 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 32%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 2 HapMap populations.
- AverageA;A 35%
- European ancestry (Utah)A;A 69%
- Yoruba (Nigeria)A;A 0%
Related
Other KDM5D SNPs
- rs2032637G;GM72+Worth knowing
- rs2032623T;TY ch haplogroup marker M60; subtree B-M60Worth knowing
- rs2032611G;GNo summary available.Typical
- rs2032612T;TNo summary available.Typical
- rs2032617T;TNo summary available.Typical
- rs2032620G;GNo summary available.Typical
- rs2032621C;CNo summary available.Typical
- rs2032622T;TNo summary available.Typical
Genosets
Genosets combine several genotypes. Twofold checks them in your report.
Source and license
Adapted from rs2032631 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.