rs4731532

GWAS Catalog Trait Associations (4)

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

systemic scleroderma

Allele A
OR 1.23
p 2.0e-12
N 25,785
Meta-analysisLarge GWAS
European

autoimmune disease

Allele A
OR
p 1.0e-10
N 59,468
Meta-analysisLarge GWAS
European

Sjogren syndrome

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele A
OR 0.23
p 1.0e-9
N 659,915
Large GWAS
multi-ancestry

blood urea nitrogen amount

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele A
OR 0.01
p 2.0e-8
N 492,819
Large GWAS
multi-ancestry

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…