rs11784833

This is a upstream gene variant variant in the GRINA gene.

GWAS Catalog Trait Associations (4)

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

level of epiplakin in blood

Allele C
OR 0.18
p 2.0e-197
N 47,745
Large GWAS
European

Red cell distribution width

Allele C
OR 0.02
p 2.0e-23
N 394,642
Large GWAS
European
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele C
OR 0.02
p 1.0e-22
N 408,112
Large GWAS
European
Allele C
OR 0.02
p 7.0e-9
N 116,666
Large GWAS
European

mean corpuscular hemoglobin

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele C
OR 0.02
p 4.0e-13
N 408,112
Large GWAS
European

low density lipoprotein cholesterol measurement

Surakka I et al. The impact of low-frequency and rare variants on lipid levels. Nature Genetics 47(6):589-97 (2015)
Allele C
OR 0.04
p 2.0e-10
N 62,166
Large GWAS
European
Hoffmann TJ et al. A large electronic-health-record-based genome-wide study of serum lipids. Nature Genetics 50(3):401-413 (2018)
Allele C
OR
β 0.027
p 2.0e-8
N 94,674
Large GWAS
multi-ancestry

About GRINA

Predicted to enable calcium channel activity. Predicted to be involved in apoptotic signaling pathway; negative regulation of extrinsic apoptotic signaling pathway via death domain receptors; and negative regulation of neuron apoptotic process. Predicted to act upstream of or within endoplasmic reticulum calcium ion homeostasis and negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway. Located in Golgi membrane. [provided by Alliance of Genome Resources, Jul 2025]

View all GRINA variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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