rs28936701(A;G)
Carrier of a primary congenital glaucoma mutation
- Magnitude
- 3.0Important
- Repute
- Bad
- Frequency
- <1%Average of 1 populations
- On SNPedia
- rs28936701(C;T)Minus strand
- Gene
- CYP1B1
Frequency
Share of people with A;G in each HapMap population.
- Luhya (Kenya)<1%
Other genotypes of rs28936701
Notes
From SNPedia
Unaffected in absence of a second CYP1B1 gene mutation
Source and license
Adapted from rs28936701(C;T) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.