rs587777149(T;T)

Inherited C59 deficiency

Magnitude
8.0Very important
Repute
Bad
On SNPedia
rs587777149(A;A)Minus strand
Gene
CD59

Other genotypes of rs587777149

  1. -;-Most notableBadinherited CD59 deficiencyVery important · 8.0
  2. -;ABadunaffected carrier of an inherited CD59 deficiency alleleVery important · 4.0
  3. A;TBadunaffected carrier of an inherited C59 deficiency alleleVery important · 4.0
  4. A;AGoodcommon in clinvarTypical · 0.0

All about rs587777149

Notes

From SNPedia

See discussion at rs587777149; however, be aware of the potential that this is an error in orientation due to ambiguous flip issues. This is a very rare inherited disorder, with a very severe phenotype, and "true" rs587777149(A;A) patients will most likely have been diagnosed early in infancy.

Source and license

Adapted from rs587777149(A;A) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.