rs8017377

This is a variant in the NYNRIN gene that changes a alanine to an threonine.

GWAS Catalog Trait Associations (3)

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

low density lipoprotein cholesterol measurement

Willer CJ et al. Discovery and refinement of loci associated with lipid levels. Nature Genetics 45(11):1274-1283 (2013)
Allele T
OR
β 0.030
p 3.0e-15
N 94,595
Large GWAS
European
Allele T
OR 0.03
p 2.0e-14
N 205,367
Large GWAS
multi-ancestry
Allele T
OR 1.17
p 4.0e-11
N 95,454
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 T
OR
β 0.036
p 2.0e-12
N 94,674
Large GWAS
multi-ancestry

total cholesterol measurement

Hoffmann TJ et al. A large electronic-health-record-based genome-wide study of serum lipids. Nature Genetics 50(3):401-413 (2018)
Allele G
OR
β 0.031
p 4.0e-10
N 94,674
Large GWAS
multi-ancestry

ClinVar annotation

Benign☆☆☆
1 submitter1 publication
View on ClinVar →

About NYNRIN

Predicted to enable RNA endonuclease activity and mRNA binding activity. Predicted to be involved in DNA integration; DNA synthesis involved in DNA repair; and DNA-templated DNA replication. Predicted to be located in membrane. Predicted to be active in cytoplasmic ribonucleoprotein granule and nucleus. [provided by Alliance of Genome Resources, Jul 2025]

View all NYNRIN variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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