rs4242384

A SNP on chromosome 8. Its most notable genotype is A;A.

Gene
None listed
Location
Chr 8127,506,309 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
12%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableNot ratedNo summary available.Typical · 0.078% 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 11 HapMap populations.

  • AverageA;A 78%
  • European ancestry (Utah)A;A 87%
  • Han Chinese (Beijing)A;A 74%
  • Japanese (Tokyo)A;A 68%
  • Yoruba (Nigeria)A;A 65%
  • African ancestry (Southwest US)A;A 75%
  • Chinese (Denver)A;A 78%
  • Gujarati IndianA;A 77%
  • Luhya (Kenya)A;A 77%
  • Mexican ancestry (Los Angeles)A;A 90%
  • Maasai (Kenya)A;A 78%
  • TuscanA;A 86%

Conditions, medicines and genes

Notes

From SNPedia

Notes

cancer-genetics these snps influence genetic risk for prostate cancer *the haplotype rs6983267 rs1016343 rs4242384 *rs7501939 *rs1859962 *rs2660753 *rs9364554 *rs6465657 *rs10993994 *rs7931342 *rs2735839 *rs5945619 *rs10993994

Source and license

Adapted from rs4242384 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.