rs3782886

A SNP in the BRAP gene on chromosome 12. Its most notable genotype is T;T: common in complete genomics

Gene
BRAP
Location
Chr 12111,672,685 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
6%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in complete genomicsTypical · 0.080% of people

SNPedia records rs3782886 on the minus strand: (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.

  • AverageT;T 80%
  • European ancestry (Utah)T;T 100%
  • Han Chinese (Beijing)T;T 72%
  • Japanese (Tokyo)T;T 58%
  • Yoruba (Nigeria)T;T 100%
  • Chinese (Denver)T;T 54%
  • Mexican ancestry (Los Angeles)T;T 98%

Conditions, medicines and genes

Notes

From SNPedia

Notes

23andMe blog coronary artery disease and heart attack SNP Risk Version Effect *rs646776 T 1.19 *rs17465637 C 1.14 *rs1746048 C 1.17 *rs6725887 C 1.17 *rs11206510 T 1.15 *rs3184504 T 1.13 *rs2306374 C 1.15 *rs3782886 C 1.44 Coronary Heart Disease

Source and license

Adapted from rs3782886 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.