rs788016

A SNP in the HSPD1 gene on chromosome 2. Its most notable genotype is A;G.

Gene
HSPD1
Location
Chr 2197,487,569 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
39%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;GMost notableNot ratedNo summary available.Typical · 0.044% of people

On SNPedia: (A;G). 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;G 44%
  • European ancestry (Utah)A;G 45%
  • Han Chinese (Beijing)A;G 31%
  • Japanese (Tokyo)A;G 48%
  • Yoruba (Nigeria)A;G 35%
  • African ancestry (Southwest US)A;G 49%
  • Chinese (Denver)A;G 43%
  • Gujarati IndianA;G 48%
  • Luhya (Kenya)A;G 43%
  • Mexican ancestry (Los Angeles)A;G 47%
  • Maasai (Kenya)A;G 50%
  • TuscanA;G 51%

Conditions, medicines and genes

Notes

From SNPedia

Notes

G-C-T-C haplotype of rs2340690-rs788016-rs2305560-rs2565163 has odds ratio of 1.91 (CI: 1.26-2.89, p=0.002) for coronary heart disease compared to G-T-T-C, based on a study of 1,000 Han Chinese patients and matched controls. * Note: Haplotype allele assignments may not be in dbSNP orientation.

Source and license

Adapted from rs788016 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.