rs28934899(G;G)

Phenyketonuria

Magnitude
6.0Very important
Repute
Bad
On SNPedia
rs28934899(G;G)
Gene
PAH

Other genotypes of rs28934899

  1. C;CGoodnormalTypical · 0.0
  2. C;GBadcarrier of Phenylketonuria alleleImportant · 3.0

All about rs28934899

Notes

From SNPedia

Two copies causes Phenylketonuria. But there is zero chance that you're learning about your own Phenylketonuria from a Promethease report. Unless Phenylketonuria is detected at birth and a strict phenylalanine-restricted diet is followed, severe medical problems would have occurred. It is more likely that you've been affected by this being an ambiguous flip but something about your data is behaving differently than from most other users. info@promethease.com would like to hear from you so that we can understand and resolve this source of confusion. March of 2015 this position was flipped in SNPedia, to be consistent with GRCh37 (at the expense of being consistent with dbSNP)

Source and license

Adapted from rs28934899(G;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.