i5012629

A SNP. Its most notable genotype is D;D: Primary Hyperoxaluria type 2

Gene
None listed
Highest magnitude
5.0Very important
Tested on
23andMe

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. D;DMost notableBadPrimary Hyperoxaluria type 2Very important · 5.0
  2. D;IBadcarrier of Primary Hyperoxaluria type 2 alleleImportant · 3.0
  3. I;IGoodcommon/normalTypical · 0.0

On SNPedia: (D;D), (D;I), (I;I). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Conditions, medicines and genes

Notes

From SNPedia

Notes

Primary hyperoxaluria type 2 Note: 23andMe may have discontinued reporting results for this SNP, as several Promethease users have reported it is not included in their data. rs180177309

Source and license

Adapted from i5012629 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.