rs11171710

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GWAS Catalog Trait Associations (7)

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

erythrocyte count

Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele A
OR 0.01
p 9.0e-13
N 394,642
Large GWAS
European

hypothyroidism

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 0.07
p 3.0e-12
N 583,911
Large GWAS
multi-ancestry

smoking cessation

Saunders GRB et al. “Genetic diversity fuels gene discovery for tobacco and alcohol use.” Nature 612(7941):720-724 (2022)
Allele A
OR 0.01
p 6.0e-10
N 1,147,272
Large GWAS
European

Peptic ulcer and gastro-oesophageal reflux disease (GORD) drug use measurement

Wu Y et al. “Genome-wide association study of medication-use and associated disease in the UK Biobank.” Nature Communications 10(1):1891 (2019)
Allele A
OR 0.05
p 3.0e-9
N 132,367
Major Consortium StudyLarge GWAS
European

gastroesophageal reflux disease

An J et al. “Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.” Nature Communications 10(1):4219 (2019)
Allele A
OR 1.03
p 1.0e-8
N 385,276
Large GWAS
European, NR

uterine fibroid

Kim J et al. “Genome-wide meta-analysis identifies novel risk loci for uterine fibroids within and across multiple ancestry groups.” Nature Communications 16(1):2273 (2025)
Allele A
OR 0.04
p 1.0e-8
N 709,132
Meta-analysisLarge 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.

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