rs11136000
CLUrs11136000 is a single-nucleotide polymorphism (SNP) in the CLU gene. Genespiral reads it in the Personality analysis to describe Mind Wandering.
- Gene
- CLU
- Alleles
- C / T
- Genotypes
- CC, TC, TT
- Traits
- 1 trait across 1 analysis
An rsID such as rs11136000 is the reference number dbSNP assigns to one position in the genome where people commonly differ by a single letter. Raw data exports from 23andMe and AncestryDNA list your two alleles at that position as a genotype - for this marker one of CC, TC, TT. The order of the two letters carries no meaning, so TC and its reverse are the same genotype.
Alleles on this page are written on the forward (plus) strand, matching how consumer raw files report them. Other references sometimes describe the same variant on the opposite strand, which swaps A↔T and C↔G - see why the same variant can look different. The associations below are educational summaries of published research; they are not diagnoses, and the effect of any single SNP is usually modest.
Mind Wandering
Cognitive Traits · Part of the Personality analysis
Related to cognitive focus and memory, influencing tendency toward daydreaming or mind-wandering.
| Genotype | Association |
|---|---|
| CC | More prone to mind wandering |
| TC | Moderate tendency |
| TT | Less prone |
- Summary
- CLU gene variations can impact attention and likelihood of mind-wandering during tasks.
- Scientific insights
- Individuals with 'CC' may find it harder to stay focused on prolonged tasks without distraction.
- Lifestyle tips
- Practicing mindfulness and setting short task intervals can help manage mind wandering.
Check your genotype at rs11136000
Load your raw DNA file and Genespiral looks up rs11136000 along with every other marker in the Personality analysis. The file is parsed in your browser and never uploaded, so your genotype stays on your device.
- 1. Download your raw data from 23andMe or AncestryDNA.
- 2. Open the analysis below and choose the file.
- 3. Find Mind Wandering in your results.
Related
References
Primary databases for this variant. Use them to check allele orientation, population frequencies, and the underlying studies.
- dbSNP entry for rs11136000 - NCBI
- rs11136000 variant page - Ensembl
- rs11136000 summary - SNPedia
- Clinical significance records for rs11136000 - ClinVar
- CLU gene - NCBI Gene
Genespiral is an educational tool, not a medical service. Genetic associations describe tendencies observed across populations, not certainties for you. Read the full disclaimer.