rs61750612(A;G)

Von Willebrand disease; carrier or Type 1

Magnitude
3.0Important
Repute
Bad
On SNPedia
rs61750612(C;T)Minus strand
Gene
VWF

Other genotypes of rs61750612

  1. G;GGoodcommon in clinvarTypical · 0.0
  2. A;AMost notableBadVon Willebrand disease, type 3Very important · 4.0

All about rs61750612

Notes

From SNPedia

Either a carrier for a Type 3 allele, or, a possible Type 1 patient; see discussion at rs61750612.

Source and license

Adapted from rs61750612(C;T) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.