rs78325861
▶GWAS Catalog Trait Associations (4)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (4)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
granzyme h 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 0.14
p 1.0e-22
N 47,745
Large GWAS
European
neutrophil percentage of leukocytes
Vuckovic D et al. “The Polygenic and Monogenic Basis of Blood Traits and Diseases.” Cell 182(5):1214-1231.e11 (2020)
Allele G
OR 0.04
p 2.0e-13
N 408,112
Large GWAS
European
type 1 diabetes mellitus
Chiou J et al. “Interpreting type 1 diabetes risk with genetics and single-cell epigenomics.” Nature 594(7863):398-402 (2021)
Allele G
OR 0.28
p 2.0e-11
N 520,580
Large GWAS
European
Crouch DJM et al. “Bayesian Effect Size Ranking to Prioritise Genetic Risk Variants in Common Diseases for Follow-Up Studies.” Genetic Epidemiology 49(1):e22608 (2025)
Allele G
OR 0.79
p 3.0e-8
N 173,981
Large GWAS
European
narcolepsy-cataplexy syndrome
Ollila HM et al. “Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy.” Nature Communications 14(1):2709 (2023)
Allele G
OR 0.33
p 3.0e-9
N 90,929
Large 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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