rs10828247
▶GWAS Catalog Trait Associations (9)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (9)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
brain attribute
van der Meer D et al. “The genetic architecture of human cortical folding.” Science Advances 7(51):eabj9446 (2021)
Allele G
OR 19.25
p 1.0e-82
N 33,748
Large GWAS
European
triple-negative breast cancer, luminal A breast carcinoma
Sun X et al. “Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants That Confer Risk for Breast Cancer.” Cancer Research 84(15):2533-2548 (2024)
Allele A
OR 0.03
p 2.0e-13
N 77,214
Large GWAS
European
breast carcinoma
Rashkin SR et al. “Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.” Nature Communications 11(1):4423 (2020)
Allele G
OR 1.09
p 3.0e-13
N 428,231
Large GWAS
European
cancer
Rashkin SR et al. “Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.” Nature Communications 11(1):4423 (2020)
Allele G
OR 1.08
p 3.0e-13
N 475,312
Large GWAS
European
cerebellar volume measurement
Moberget T et al. “The genetic architecture of human cerebellar morphology supports a key role for the cerebellum in human evolution and psychopathology.” Communications Biology 9(1) (2026)
Allele G
OR —
p 1.0e-12
N 27,302
Large GWAS
European
waist-hip ratio
Pulit SL et al. “Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry.” Human Molecular Genetics 28(1):166-174 (2019)
Allele A
OR 0.01
p 2.0e-12
N 316,772
Meta-analysisLarge GWAS
European
normal pressure hydrocephalus
Räsänen J et al. “Risk Variants Associated With Normal Pressure Hydrocephalus: Genome-Wide Association Study in the FinnGen Cohort.” Neurology 103(5):e209694 (2024)
Allele G
OR 0.26
p 6.0e-12
N 452,613
Major Consortium StudyLarge GWAS
European
osteoarthritis
Hatzikotoulas K et al. “Translational genomics of osteoarthritis in 1,962,069 individuals.” Nature 641(8065):1217-1224 (2025)
Allele A
OR 0.98
p 2.0e-10
N 1,962,069
Large GWAS
multi-ancestry
migraine disorder
Hautakangas H et al. “Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles.” Nature Genetics 54(2):152-160 (2022)
Allele G
OR 1.03
p 8.0e-9
N 873,341
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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