rs17089782(A;G)
Carrier of a Joubert syndrome 33 mutation
- Magnitude
- 3.0Important
- Repute
- Bad
- Frequency
- 7%Average of 9 populations
- On SNPedia
- rs17089782(A;G)
- Gene
- PIBF1
Frequency
Share of people with A;G in each HapMap population.
- Mexican ancestry (Los Angeles)21%
- Chinese (Denver)12%
- Han Chinese (Beijing)9%
- Tuscan7%
- Gujarati Indian5%
- African ancestry (Southwest US)4%
- Japanese (Tokyo)2%
- European ancestry (Utah)2%
- Yoruba (Nigeria)0%
Other genotypes of rs17089782
Notes
From SNPedia
Unaffected in absence of a second PIBF1 gene mutation
Source and license
Adapted from rs17089782(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.