rs1057519337(T;T)

Alport syndrome; most likely in males due to X-linkage

Magnitude
5.8Very important
Repute
Bad
On SNPedia
rs1057519337(A;A)Minus strand
Gene
AMMECR1

Other genotypes of rs1057519337

  1. C;TBadCarrier of an Alport syndrome mutation; X-linkedImportant · 3.0
  2. C;CGoodcommon/normalTypical · 0.0

All about rs1057519337

Notes

From SNPedia

Likely to have a form of Alport syndrome; see discussion there and at rs1057519337

Source and license

Adapted from rs1057519337(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.