rs12325192

GWAS Catalog Trait Associations (3)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

uterine prolapse

Allele C
OR 1.17
p 2.0e-23
N 234,621
Large GWAS
European
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.15
p 1.0e-14
N 317,583
Large GWAS
multi-ancestry

pelvic organ prolapse

Allele T
OR 0.89
p 1.0e-21
N 574,377
Large GWAS
European
Allele T
OR 1.12
p 3.0e-12
N 355,744
Major Consortium StudyLarge GWAS
European

Uterine leiomyoma

Allele C
OR 1.07
p 4.0e-12
N 295,291
Large GWAS
European

This variant is in our database but has no known associations or PRS memberships yet.

Gene information from NCBI Gene. Variant classifications from ClinVar.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Sign in to join the discussion.

Loading comments…