rs373145711(C;C)

Common in clinvar

Magnitude
0.0Typical
Repute
Good
On SNPedia
rs373145711(C;C)
Gene
ASXL1

Other genotypes of rs373145711

  1. C;TMost notableBadBohring-Opitz syndromeVery important · 8.0

All about rs373145711

Source and license

Adapted from rs373145711(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.