rs34690599(C;G)

Beta Thalassemia carrier; Hemoglobin beta-plus mutation

Magnitude
3.0Important
Repute
Bad
On SNPedia
rs34690599(C;G)Minus strand
Gene
HBB

Other genotypes of rs34690599

  1. G;GGoodcommon in clinvarTypical · 0.0
  2. C;CMost notableBadBeta Thalassemia intermedia likely; Hemoglobin beta-plus; variable clinical symptomsVery important · 4.5

All about rs34690599

Notes

From SNPedia

Unaffected in absence of a second HBB gene mutation; see discussion at HBB

Source and license

Adapted from rs34690599(C;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.