rs137852946(C;T)

Carrier of a possible polycystic kidney disease allele

Magnitude
3.0Important
Repute
Bad
On SNPedia
rs137852946(A;G)Minus strand
Gene
PKHD1

Other genotypes of rs137852946

  1. T;TMost notableBadpossible polycystic kidney diseaseVery important · 6.0
  2. C;CGoodcommon in clinvarTypical · 0.0

All about rs137852946

Notes

From SNPedia

It is unclear if this risk allele (T) has been seen leading to polycystic kidney disease (when present in homozygous or compound heterozygous form) in more than one patient. Please feel free to contact SNPedia if you have additional information about this allele.

Source and license

Adapted from rs137852946(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.