rs17601876
▶GWAS Catalog Trait Associations (7)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (7)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
body height
Yengo L et al. “A saturated map of common genetic variants associated with human height.” Nature 610(7933):704-712 (2022)
Allele A
OR 0.02
p 1.0e-42
N 5,314,291
Large GWAS
European, Hispanic or Latin American, East Asian, African unspecified, South Asian
endometrial cancer
Ramachandran D et al. “GWAS meta-analysis identifies five susceptibility loci for endometrial cancer.” Ebiomedicine 118:105830 (2025)
Allele A
OR 0.89
p 2.0e-18
N 306,458
Meta-analysisLarge GWAS
multi-ancestry
endometrial cancer, COVID-19
Zhao X et al. “A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers.” Iscience 26(9):107497 (2023)
Allele G
OR —
p 3.0e-14
N 2,217,228
Large GWAS
European
IGF-1 measurement
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele G
OR 0.01
p 5.0e-14
N 394,642
Large GWAS
European
estradiol measurement
Pott J et al. “Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease.” The Journal of Clinical Endocrinology and Metabolism 104(11):5008-5023 (2019)
Allele G
OR 0.07
p 5.0e-13
N 6,798
Large GWAS
European
body composition measurement
Wu Z et al. “Genetic architecture of bone marrow fat fraction implies its involvement in osteoporosis risk.” Nature Communications 16(1):7490 (2025)
Allele G
OR 0.04
p 3.0e-9
N 39,178
Large GWAS
European
endometrial carcinoma
O'Mara TA et al. “Identification of nine new susceptibility loci for endometrial cancer.” Nature Communications 9(1):3166 (2018)
Allele G
OR 1.12
p 2.0e-10
N 54,884
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.
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