rs10186870 (LINC01824): Educational Attainment SNP

Key takeaways

  • rs10186870 lies in the LINC01824 / MIR7515HG non-coding RNA region and was genome-wide significant for educational attainment in approximately 3 million participants.
  • It is one of 3,952 independent educational attainment variants; no individual effect size for this SNP is available from the provided study text.
  • A polygenic index from all 3,952 variants explains 12 to 16 percent of variance in educational attainment in held-out samples.
  • Direct genetic effects, after removing family environment influence, account for roughly half the polygenic index's predictive power for educational attainment.
  • Couples share more similar genetic profiles for educational attainment than expected from matching on education level, suggesting selection on related traits.

Key takeaways

  • rs10186870 lies within the LINC01824 / MIR7515HG non-coding RNA region and was identified as genome-wide significant for educational attainment in one of the largest genetic studies to date (approximately 3 million participants).
  • It is one of 3,952 independent variants tied to educational attainment in this study; no individual effect size for rs10186870 is available in the provided study text.
  • A polygenic index built from all 3,952 associated variants explains 12 to 16 percent of variance in educational attainment across held-out validation samples.
  • After accounting for parental genetics, direct effects explain roughly half the polygenic index's predictive association with educational attainment and other traits.
  • Couples share more similar polygenic profiles for educational attainment than expected from matching on education level alone, suggesting assortative mating on additional related factors.

What the research says rs10186870 is located within LINC01824 (Long Intergenic Non-Protein Coding RNA 1824) and MIR7515HG (the host gene for microRNA 7515), two non-coding RNA genes. The variant was among 3,952 approximately uncorrelated genome-wide-significant single-nucleotide polymorphisms (single-letter differences in the DNA sequence, also called SNPs) identified in a genome-wide association study (GWAS, a method that tests hundreds of thousands of genetic variants across many people to find statistical links with a trait) of educational attainment (EA) spanning approximately 3,037,499 individuals. A polygenic index (a score that sums the small contributions of many variants) built from these signals explains 12 to 16 percent of variance in EA across validation samples, roughly a 20 percent improvement over the prior study in the same research series. Direct effects, estimated within families by controlling for parental polygenic indices, account for roughly half that association with this trait and other phenotypes, while mate-pair polygenic index correlations were far larger than expected from phenotypic assortment alone.

Reported associations

  • Educational attainment (years of schooling completed): Listed among 3,952 genome-wide-significant variants for EA in a GWAS of approximately 3,037,499 individuals; no individual effect size for rs10186870 is reported in the available study text.

Evidence quality The association originates from the EA4 meta-analysis (a combined analysis pooling results from multiple cohorts), the fourth and largest iteration of this research program, with approximately 3,037,499 participants. The series has grown from roughly 126,559 individuals in the first iteration to the current scale, with the polygenic index R-squared (the percentage of variance explained) rising from approximately 2.6 percent to 12 to 16 percent over that period. The mean test statistic for the autosomal EA4 GWAS was 4.90, reflecting a well-powered study. No individual effect size for rs10186870 is provided in the available study text, and no dedicated replication for this specific variant is described. A dominance analysis (testing whether carrying two copies of a variant differs from the additive prediction) identified no genome-wide-significant signals for any EA variant, suggesting the additive model fits well across this trait. Because educational attainment reflects environmental, cultural, and socioeconomic factors in addition to genetics, the biological interpretation of any single EA-associated variant, including this locus, remains preliminary and should be interpreted with caution.

Lifestyle considerations No lifestyle considerations on file for this variant.

Frequently asked questions

What is rs10186870?

rs10186870 is a single-nucleotide polymorphism (a single-letter DNA variation) located within the LINC01824 and MIR7515HG non-coding RNA genes. It was identified as genome-wide significant for educational attainment in a study of approximately 3 million individuals.

What is LINC01824?

LINC01824 stands for Long Intergenic Non-Protein Coding RNA 1824, indicating it is a gene that produces an RNA molecule rather than a protein. The specific biological role of LINC01824 in relation to educational attainment is not described in the available study.

Is rs10186870 an intelligence gene?

The research studied educational attainment (years of schooling completed), not intelligence directly. Educational attainment is shaped by many environmental and social factors in addition to genetics, so rs10186870 should not be interpreted as an intelligence gene.

What is a polygenic index for educational attainment?

A polygenic index combines the small effects of thousands of genetic variants, including rs10186870, into a single summary score. The index built in this study explains 12 to 16 percent of the differences in years of schooling across individuals in held-out validation samples.

How reliable is the genetic link between rs10186870 and educational attainment?

The association comes from one of the largest GWAS studies ever conducted (approximately 3 million individuals), which is a notable strength. However, no individual effect size for rs10186870 is available in the study text, educational attainment is heavily influenced by environment, and the biological meaning of this specific variant remains preliminary.