rs5945572

A SNP on chromosome X. Its most notable genotype is A;A.

Gene
None listed
Location
Chr X51,486,831 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
24%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableNot ratedNo summary available.Typical · 0.014% of people

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 6 HapMap populations.

  • AverageA;A 14%
  • European ancestry (Utah)A;A 32%
  • Han Chinese (Beijing)A;A <1%
  • Japanese (Tokyo)A;A 5%
  • Yoruba (Nigeria)A;A 25%
  • Chinese (Denver)A;A 6%
  • Luhya (Kenya)A;A 12%

Conditions, medicines and genes

Notes

From SNPedia

Notes

Associated with prostate cancer Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium. Generalizability of associations from prostate cancer genome-wide association studies in multiple populations. Replication of the 10q11 and Xp11 prostate cancer risk variants: results from a Utah pedigree-based study. Meta-analysis of genome-wide and replication association studies on prostate cancer. Validation of genome-wide prostate cancer associations in men of African descent. Characterizing associations and SNP-environment interactions for GWAS-identified prostate cancer risk markers--results from BPC3.

Source and license

Adapted from rs5945572 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.