rs11031002
▶GWAS Catalog Trait Associations (6)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (6)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
blood protein amount
Gudjonsson A et al. “A genome-wide association study of serum proteins reveals shared loci with common diseases.” Nature Communications 13(1):480 (2022)
Allele A
OR 0.16
p 5.0e-20
N 5,368
Large GWAS
European
body height
Schoeler T et al. “Combining cross-sectional and longitudinal genomic approaches to identify determinants of cognitive and physical decline.” Nature Communications 16(1):4524 (2025)
Allele T
OR 0.01
p 5.0e-14
N 405,540
Large GWAS
European
health trait
Schoeler T et al. “Combining cross-sectional and longitudinal genomic approaches to identify determinants of cognitive and physical decline.” Nature Communications 16(1):4524 (2025)
Allele T
OR 0.01
p 1.0e-9
N 405,979
Large GWAS
European
polycystic ovary syndrome
Pujol Gualdo N et al. “Atlas of genetic and phenotypic associations across 42 female reproductive health diagnoses.” Nature Medicine 31(5):1626-1634 (2025)
Allele T
OR 0.83
p 2.0e-9
N 288,356
Large GWAS
European
Tyrmi JS et al. “Leveraging Northern European population history: novel low-frequency variants for polycystic ovary syndrome.” Human Reproduction (oxford, England) 37(2):352-365 (2022)
Allele T
OR 1.24
p 9.0e-9
N 141,355
Large GWAS
European
hormone measurement, Luteinizing hormone level
Ruth KS et al. “Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes.” European Journal of Human Genetics : Ejhg 24(2):284-90 (2016)
Allele A
OR 0.22
p 4.0e-9
N 2,913
Large GWAS
European
amenorrhea
Pujol Gualdo N et al. “Atlas of genetic and phenotypic associations across 42 female reproductive health diagnoses.” Nature Medicine 31(5):1626-1634 (2025)
Allele T
OR 0.87
p 1.0e-8
N 222,924
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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