rs117911120 (SERPINB10): Adolescent Cognitive GWAS

Key takeaways

  • rs117911120 appeared in a genome-wide study of adolescent cognitive traits but did not reach conventional statistical significance
  • Genetics as a group explain roughly 30% of working memory differences and 19% of processing speed differences among adolescents in this cohort
  • No single variant was pinpointed as a significant driver of working memory, processing speed, or inhibitory control
  • Working memory showed genetic overlap with general intelligence and academic attainment at the population level
  • Evidence for this specific variant is preliminary, from a single cohort of about 4,600 adolescents with no reported independent replication

Key takeaways

  • rs117911120 appeared in a genome-wide study of adolescent cognitive traits but did not reach conventional statistical significance in a sample of 4,611 adolescents
  • Genetics as a group explain roughly 30% of working memory differences and 19% of processing speed differences among adolescents in this cohort
  • No single variant was pinpointed as a significant driver of working memory, processing speed, or inhibitory control in this study
  • Working memory showed genetic overlap with general intelligence and academic attainment at the population level
  • Evidence for this specific variant is preliminary and comes from a single cohort without reported independent replication

What the research says A genome-wide association study (GWAS, a scan of hundreds of thousands of genetic variants across the genome to find ones linked to a trait) examined working memory (WM, the ability to hold and mentally manipulate information), inhibitory control (IC, the ability to resist impulses), and processing speed (PS, how quickly a person responds to stimuli) in 4,611 adolescents from the Avon Longitudinal Study of Parents and Children (ALSPAC); no loci reached genome-wide significance (the conventional threshold of p < 5 x 10^-8), so rs117911120 did not clear that bar. At the aggregate level, common genetic variants collectively explained approximately 30% of latent WM variance and 19% of PS variance in this cohort, while no significant collective genetic contribution was detected for IC. The study further identified significant genetic correlations (a statistical measure of shared inherited architecture between traits at the population level, distinct from a direct variant-to-trait link) between WM and both general intelligence and academic attainment, and a more modest genetic overlap between PS and intelligence.

Reported associations

  • Working memory (latent factor combining multiple tasks): Studied as a primary trait in 4,611 ALSPAC adolescents; no individual variant including rs117911120 reached genome-wide significance; common single nucleotide polymorphisms (SNPs, single-letter differences in DNA) collectively explained approximately 30% of variance
  • Processing speed: Studied in the same cohort; no individual variant reached genome-wide significance; common SNPs collectively explained approximately 19% of variance
  • Inhibitory control: Studied in the same cohort; no significant common genetic contribution was detected for this trait
  • General intelligence and academic attainment: Significant genetic correlations with WM were identified at the aggregate level, indicating overlapping inherited architecture across these traits in the population; a more modest overlap was found between PS and intelligence

Evidence quality The sole study contributing evidence in this entry enrolled 4,611 adolescents from a single UK birth cohort (ALSPAC), substantially smaller than the 50,000 or more participants typically required to reliably detect individual SNP effects on cognitive traits with high confidence. No locus reached genome-wide significance (p < 5 x 10^-8). No replication of any finding in an independent sample is reported in the available text. The authors examined genetic overlap with ADHD in addition to intelligence and academic attainment, though full results for that comparison were not available in the provided excerpt. The aggregate-level genetic correlations add biological context about shared architecture across cognitive traits but do not confirm any specific variant association. Evidence for rs117911120 as a trait-associated variant is therefore preliminary and should be interpreted with caution.

Lifestyle considerations No lifestyle considerations on file for this variant.

Frequently asked questions

What is the SERPINB10 gene?

SERPINB10 is a gene located near the rs117911120 variant. The study associated with this entry examined cognitive performance in adolescents but did not describe specific cellular functions of SERPINB10 itself.

Is rs117911120 linked to memory or intelligence?

rs117911120 appeared in a genome-wide study of working memory and processing speed in adolescents but did not reach statistical significance. No confirmed link between this specific variant and any cognitive trait has been established.

What is working memory and why is it studied genetically?

Working memory is the ability to hold and mentally manipulate information over short periods. It predicts academic performance and is linked to general intelligence, making it a target for genetic research into why people differ in thinking and learning.

What did the ALSPAC adolescent cognitive GWAS find?

The study of 4,611 adolescents found that common genetic variants as a group explained about 30% of working memory variance and 19% of processing speed variance, but no single genomic variant reached genome-wide significance. No significant genetic contribution was found for inhibitory control.

How reliable is the evidence for rs117911120?

The evidence is preliminary. It comes from one study of about 4,600 adolescents, the variant did not reach genome-wide significance, and no independent replication has been reported. Larger studies across multiple cohorts would be needed to confirm any association.