rs147394623(A;G)

Carrier of a retinitis pigmentosa (RP) mutation

Magnitude
3.0Important
Repute
Bad
On SNPedia
rs147394623(A;G)
Gene
DHDDS

Other genotypes of rs147394623

  1. A;AGoodcommon in clinvarTypical · 0.0
  2. G;GMost notableBadRetinitis pigmentosa, type 59Very important · 4.4

All about rs147394623

Notes

From SNPedia

Unaffected in absence of another DHDDS gene mutation; see discussion at rs147394623.

Source and license

Adapted from rs147394623(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.