rs2576159

This is a intron variant variant in the RNLS gene.

GWAS Catalog Trait Associations (2)

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

hematocrit

Allele T
OR 0.01
p 6.0e-12
N 562,259
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 T
OR 0.02
p 3.0e-11
N 408,112
Large GWAS
European

hemoglobin measurement

Allele T
OR 0.01
p 2.0e-11
N 928,679
Large GWAS
multi-ancestry
Allele T
OR
p 2.0e-10
N 746,431
Large GWAS
multi-ancestry
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.01
p 9.0e-9
N 502,921
Large GWAS
multi-ancestry
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele T
OR 0.02
p 1.0e-11
N 408,112
Large GWAS
European

About RNLS

Enables several functions, including NADH binding activity; epinephrine binding activity; and monoamine oxidase activity. Involved in negative regulation of blood pressure and negative regulation of heart rate. Located in extracellular region. Implicated in essential hypertension and hypertension. Biomarker of end stage renal disease. [provided by Alliance of Genome Resources, Jul 2025]

View all RNLS variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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