rs61750612(G;G)

Common in clinvar

Magnitude
0.0Typical
Repute
Good
On SNPedia
rs61750612(C;C)Minus strand
Gene
VWF

Other genotypes of rs61750612

  1. A;GBadVon Willebrand disease; carrier or Type 1Important · 3.0
  2. A;AMost notableBadVon Willebrand disease, type 3Very important · 4.0

All about rs61750612

Source and license

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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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