rs35923643

This is a regulatory region variant variant in the GRAMD1B gene.

GWAS Catalog Trait Associations (12)

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

chronic lymphocytic leukemia

Allele G
OR 1.63
p 4.0e-58
N 17,691
Large GWAS
European
Allele G
OR 1.66
p 2.0e-40
N 10,767
Meta-analysisLarge GWAS
multi-ancestry

CD5 antigen-like measurement

Allele G
OR 0.08
p 6.0e-35
N 47,745
Large GWAS
European

annexin A1 measurement

Allele G
OR 0.08
p 6.0e-27
N 47,745
Large GWAS
European

level of protein ZNRD2 in blood

Allele G
OR 0.07
p 4.0e-25
N 47,745
Large GWAS
European

blood protein amount

Allele G
OR 0.04
p 1.0e-17
N 47,745
Large GWAS
European

fas apoptotic inhibitory molecule 3 measurement

Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele A
OR 0.13
p 2.0e-15
N 10,708
Large GWAS
European

lymphocyte percentage of leukocytes

Allele G
OR 0.02
p 1.0e-14
N 394,642
Large GWAS
European

About GRAMD1B

Predicted to enable cholesterol binding activity; cholesterol transfer activity; and phospholipid binding activity. Predicted to be involved in cellular response to cholesterol; cholesterol homeostasis; and intracellular sterol transport. Located in endoplasmic reticulum membrane; endoplasmic reticulum-plasma membrane contact site; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]

View all GRAMD1B variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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