rs12428625

GWAS Catalog Trait Associations (1)

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

Hirschsprung disease

Fadista J et al. Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus. European Journal of Human Genetics : Ejhg 26(4):561-569 (2018)
Allele T
OR 3.63
p 4.0e-11
N 4,887
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…