rs71413877

This is a intron variant variant in the LONRF2 gene.

GWAS Catalog Trait Associations (4)

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

intelligence

Allele A
OR 0.06
p 5.0e-13
N 248,482
Large GWAS
European
Allele A
OR 5.97
p 2.0e-9
N 300,486
Large GWAS
European
Allele A
OR 6.28
p 3.0e-10
N 269,867
Meta-analysisLarge GWAS
European
Allele A
OR 0.04
p 2.0e-9
N 254,641
Large GWAS
European

mathematical ability

Allele A
OR 0.03
p 6.0e-13
N 811,539
Large GWAS
European

household income

Allele A
OR 0.04
p 7.0e-13
N 505,541
Large GWAS
European, NR

self reported educational attainment

Allele A
OR 0.04
p 3.0e-22
N 1,131,881
Large GWAS
European
Allele A
OR
β 0.035
p 2.0e-9
N 405,072
Large GWAS
European

About LONRF2

Predicted to enable misfolded protein binding activity; ribonucleoprotein complex binding activity; and ubiquitin protein ligase activity. Predicted to act upstream of or within several processes, including motor behavior; neuron differentiation; and protein quality control for misfolded or incompletely synthesized proteins. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]

View all LONRF2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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