rs6850524
CSNK1Ers6850524 is a single-nucleotide polymorphism (SNP) in the CSNK1E gene. Genespiral reads it in the Sleep analysis to describe Jet Lag Recovery.
- Gene
- CSNK1E
- Alleles
- A / G
- Genotypes
- AA, AG, GG
- Traits
- 1 trait across 1 analysis
An rsID such as rs6850524 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 AA, AG, GG. The order of the two letters carries no meaning, so AG 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.
Jet Lag Recovery
Sleep Patterns · Part of the Sleep analysis
Influences circadian adjustment, impacting recovery time from jet lag.
| Genotype | Association |
|---|---|
| AA | Faster recovery from jet lag |
| AG | Moderate recovery time |
| GG | Slower recovery from jet lag |
- Summary
- CSNK1E gene variations may determine an individual’s resilience to jet lag.
- Scientific insights
- 'AA' individuals tend to adjust more quickly to new time zones than 'GG' individuals.
- Lifestyle tips
- Gradually adjusting sleep times before travel can help mitigate jet lag.
Check your genotype at rs6850524
Load your raw DNA file and Genespiral looks up rs6850524 along with every other marker in the Sleep 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 Jet Lag Recovery in your results.
Related
More markers from Sleep
References
Primary databases for this variant. Use them to check allele orientation, population frequencies, and the underlying studies.
- dbSNP entry for rs6850524 - NCBI
- rs6850524 variant page - Ensembl
- rs6850524 summary - SNPedia
- Clinical significance records for rs6850524 - ClinVar
- CSNK1E 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.