rs2155219

This is a regulatory region variant variant.

GWAS Catalog Trait Associations (10)

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

eosinophil count

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.03
p 3.0e-68
N 442,919
Large GWAS
multi-ancestry

Crohn's disease

Allele A
OR 1.19
p 6.0e-46
N 20,883
Large GWAS
multi-ancestry

inflammatory bowel disease

Allele T
OR 1.15
p 4.0e-36
N 34,366
Large GWAS
European

ulcerative colitis

Allele T
OR 1.13
p 8.0e-21
N 27,432
Large GWAS
multi-ancestry
Allele T
OR 1.13
p 5.0e-16
N 26,405
Meta-analysisLarge GWAS
European

allergic disease

Allele T
OR 0.11
p 2.0e-19
N 53,862
Meta-analysisLarge GWAS
European

allergic sensitization measurement

Allele T
OR 1.18
p 1.0e-18
N 15,845
Meta-analysisLarge GWAS
European

atopic eczema, childhood onset asthma, atopic march

Allele T
OR 1.33
p 2.0e-15
N 11,181
Meta-analysisLarge GWAS
European

asthma

Allele T
OR 0.11
p 3.0e-15
N 127,669
Large GWAS
European

seasonal allergic rhinitis

Allele T
OR 1.22
p 1.0e-8
N 12,347
Meta-analysisLarge GWAS
European

alopecia areata

Allele T
OR 1.21
p 4.0e-8
N 7,565
Meta-analysis
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…