rs7090530

GWAS Catalog Trait Associations (4)

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

autoimmune thyroid disease

Allele A
OR 1.10
p 2.0e-26
N 754,406
Large GWAS
European
Zeng Y et al. Genetic Associations Between Stress-Related Disorders and Autoimmune Disease. The American Journal of Psychiatry 180(4):294-304 (2023)
Allele A
OR 0.91
p 3.0e-18
N 376,871
Large GWAS
European

Thyroid preparation use measurement

Allele C
OR 0.09
p 7.0e-24
N 305,582
Major Consortium StudyLarge 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 0.08
p 1.0e-21
N 484,308
Large GWAS
multi-ancestry

hypothyroidism

Allele A
OR 0.06
p 5.0e-52
N 1,786,062
Large GWAS
European
Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.05
p 1.0e-14
N 626,668
Major Consortium StudyLarge GWAS
multi-ancestry
Allele A
OR 0.08
p 9.0e-19
N 394,626
Large GWAS
European

Research that mentions this SNP (1)

Possible contribution of GSTP1 and other xenobiotic metabolizing genes to vitiligo susceptibility
AssociationN=200Mikhail M. Minashkin et al.(2013)· Archives of Dermatological Research

A candidate gene association study in 100 Russian vitiligo patients and 100 controls identified a strong novel association between GSTP1 rs1138272 (Ala114Val, OR=13.03, Bonferroni-adjusted P=0.0015) and vitiligo susceptibility. Cumulative analysis of multiple xenobiotic metabolizing genes showed that carrying higher numbers of risk alleles was associated with increased vitiligo risk (9-16 vs 3-8 alleles: OR=2.79, P=0.00063), supporting a polygenic model for vitiligo involving detoxification pathway genes.

Traits studied:Vitiligo

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…