rs812426

This variant is located in the RSU1 gene.

GWAS Catalog Trait Associations (4)

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

protein FAM163B measurement

Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele C
OR 0.51
p
N 10,708
Large GWAS
European

platelet component distribution width

Allele G
OR 0.03
p 3.0e-57
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 G
OR 0.04
p 8.0e-54
N 408,112
Large GWAS
European

platelet count

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele C
OR 0.03
p 3.0e-27
N 407,168
Major Consortium StudyLarge GWAS
European
Allele C
OR
p 3.0e-14
N 721,201
Large GWAS
multi-ancestry
Allele C
OR 0.01
p 2.0e-12
N 394,642
Large GWAS
European

platelet crit

Allele G
OR 0.02
p 8.0e-22
N 394,642
Large GWAS
European

About RSU1

This gene encodes a protein that is involved in the Ras signal transduction pathway, growth inhibition, and nerve-growth factor induced differentiation processes, as determined in mouse and human cell line studies. In mouse, the encoded protein was initially isolated based on its ability to inhibit v-Ras transformation. Multiple alternatively spliced transcript variants for this gene have been reported; one of these variants was found only in glioma tumors. [provided by RefSeq, Jul 2008]

View all RSU1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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