rs1057519337(C;T)

Carrier of an Alport syndrome mutation; X-linked

Magnitude
3.0Important
Repute
Bad
On SNPedia
rs1057519337(A;G)Minus strand
Gene
AMMECR1

Other genotypes of rs1057519337

  1. T;TMost notableBadAlport syndrome; most likely in males due to X-linkageVery important · 5.8
  2. C;CGoodcommon/normalTypical · 0.0

All about rs1057519337

Notes

From SNPedia

Mothers with this genotype are unaffected but have a 50% chance of having an affected son; see discussion at rs1057519337 and at Alport syndrome.

Source and license

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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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