rs17602729(C;G)

Unexpected genotype

Magnitude
2.1Worth knowing
Repute
Not rated
Frequency
0%Average of 9 populations
On SNPedia
rs17602729(C;G)Minus strand
Gene
AMPD1

Frequency

Share of people with C;G in each HapMap population.

  • European ancestry (Utah)0%
  • Han Chinese (Beijing)0%
  • Japanese (Tokyo)0%
  • Yoruba (Nigeria)0%
  • Gujarati Indian0%
  • Luhya (Kenya)0%
  • Mexican ancestry (Los Angeles)0%
  • Maasai (Kenya)0%
  • Tuscan0%

Other genotypes of rs17602729

  1. T;TBadAMPD1 deficiency homozygous (orientation reversed)Important · 3.00% of people
  2. G;TNot ratedunexpected genotypeWorth knowing · 2.10% of people
  3. C;TBadAMPD1 deficiency heterozygous (orientation reversed)Worth knowing · 2.80% of people
  4. A;TMost notableNot ratedReally unexpected!Important · 3.50% of people
  5. G;GGoodnormalTypical · 0.094% of people
  6. A;GBadAMPD1 deficiency heterozygousWorth knowing · 2.85% of people
  7. C;CGoodnormal (orientation reversed)Typical · 0.00% of people
  8. A;CNot ratedunexpected genotypeImportant · 3.40% of people
  9. A;ABadAMPD1 deficiency homozygousImportant · 3.0<1% of people

All about rs17602729

Notes

From SNPedia

please self report to info@snpedia.com

Source and license

Adapted from rs17602729(C;G) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.