rs17602729(C;T)

AMPD1 deficiency heterozygous (orientation reversed)

Magnitude
2.8Worth knowing
Repute
Bad
Frequency
0%Average of 9 populations
On SNPedia
rs17602729(A;G)Minus strand
Gene
AMPD1

Frequency

Share of people with C;T 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. A;TMost notableNot ratedReally unexpected!Important · 3.50% of people
  4. G;GGoodnormalTypical · 0.094% of people
  5. C;GNot ratedunexpected genotypeWorth knowing · 2.10% 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

If orientation is incorrect in your raw data, this would be the pathogenic heterozygous allele. This SNP changed orientation between b36 and b37. See rs17602729(C;T) for the new orientation.

Source and license

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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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