rs9525638

A SNP on chromosome 13. Its most notable genotype is C;C: stronger bones

Gene
None listed
Location
Chr 1342,554,441 (GRCh38)
Highest magnitude
2.0Worth knowing
Tested on
23andMe, AncestryDNA
Minor allele frequency
37%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodstronger bonesWorth knowing · 2.011% of people
  2. T;TBadweaker bonesWorth knowing · 2.044% of people

On SNPedia: (C;C), (T;T). 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;C 11% T;T 44%
  • European ancestry (Utah)C;C 21% T;T 30%
  • Han Chinese (Beijing)C;C 23% T;T 31%
  • Japanese (Tokyo)C;C 11% T;T 35%
  • Yoruba (Nigeria)C;C 3% T;T 61%
  • African ancestry (Southwest US)C;C 2% T;T 65%
  • Chinese (Denver)C;C 13% T;T 34%
  • Gujarati IndianC;C 13% T;T 32%
  • Luhya (Kenya)C;C 7% T;T 59%
  • Mexican ancestry (Los Angeles)C;C 14% T;T 38%
  • Maasai (Kenya)C;C 6% T;T 60%
  • TuscanC;C 14% T;T 35%

Conditions, medicines and genes

Notes

From SNPedia

Notes

Osteoporosis

Source and license

Adapted from rs9525638 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.