Traits - Genetic associations studied in anxiety-response research

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Genetic associations studied in anxiety-response research

General

This research area looks at the anxiety and tension component of neuroticism, a Big Five personality dimension.

GWAS work has identified variants linked to self-reported anxiety and tension, with overlap with broader neuroticism, depression, and well-being traits.

This result reflects research-level variation in personality-related traits and is not a clinical anxiety diagnosis.

Stress, sleep, life events, relationships, mental health support, and overall context strongly shape how anxiety actually appears.

Selected sample
Demo Report
Report markers
20 SNP entries
Genes
0
Research
1 study
Research summary

What this trait studies

Research summary, not an individual result

This trait is presented as population-level genetic research rather than an individual Low/High verdict, because the science behind it is either too preliminary, too easily misread as a diagnosis, or too sensitive to responsibly reduce to a single badge.

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Explore the evidence

Behind this report

Review the genes, tested markers and supporting research.

SNPs tested

These are the unique genetic markers analyzed for this trait. Genotypes showing "--" were not identified in your DNA file. Report marker totals can include repeated study entries; this table shows each SNP once.

Genotypes and reported variant frequencies
SNPChromosomeGenotypeVariant alleleFrequency
rs3764002CTT25.70%
rs7526108GA23.54%
rs9829032AGG38.10%
rs10027492--42.35%
rs11030088--A12.30%
rs17175643--78.89%
rs2458604--A40.02%
rs28570522--39.26%
rs3800227--46.91%
rs3902934--57.57%
rs4129585--23.88%
rs8054556--60.54%
rs10174328--72.58%
rs2071044--44.73%
rs2672852--45.61%
rs4856278--16.75%
rs76508707--T45.33%
rs7652808--24.26%
rs77165542--98.96%
rs9828679--C11.28%

DNA Genics reports genotypes based on the 'positive' strand of the human genome reference sequence (build 37/HG19). Other companies may use the opposite strand, so genotypes may need conversion for comparison.

Research studies

The following peer-reviewed scientific studies support the genetic associations analyzed in this report.

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Coverage: 3/20 SNP entries detected (15%).

Reference: Human Genome Build 37 (HG19). Other testing companies may report using the opposite strand, requiring conversion for comparison.

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