i5012628
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.
- D;DMost notableBadPrimary hyperoxaluria type 2
- D;IBadcarrier of Primary hyperoxaluria type 2 allele
- I;IGoodcommon/normal
On SNPedia: (D;D), (D;I), (I;I). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
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. rs80356708
Source and license
Adapted from i5012628 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.