Traits - Tension tendency

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Tension tendency

General

This trait reflects a UK Biobank self-report item about how often someone feels tense, used in mood and personality research.

GWAS work has identified variants linked to this self-report, with overlap with anxiety and neuroticism.

This result reflects research-level variation in mood-related traits and is not a clinical assessment.

Stress, sleep, life events, mental health support, and current context strongly shape how tense someone feels.

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Report markers
33 SNP entries
Genes
0
Research
1 study
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Genetic association

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Average genetic tendency

This is a weak, population-level genetic association, not a personal diagnosis or a definitive trait.

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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
rs4671330AAA33.54%
rs7194615CCC44.85%
rs9527336AAA27.72%
rs9811546GAA31.20%
rs10068637--A27.61%
rs10218528--A40.06%
rs10228350--41.29%
rs10767733--A40.28%
rs11090045--A30.23%
rs1147851--G28.46%
rs11509880--A34.42%
rs144851691--T0.41%
rs1450832--A29.01%
rs17291908--47.58%
rs2067919--34.36%
rs2071802--G11.06%
rs2097247--T9.58%
rs2100888--A36.56%
rs2217250--G20.85%
rs28738966--A21.74%
rs2937336--A27.84%
rs3171692--T32.95%
rs3740393--C14.06%
rs3751855--39.39%
rs4129585--42.67%
rs4937872--41.70%
rs5019341--C24.16%
rs56084168--T14.80%
rs6883228--C18.32%
rs6891955--C35.42%
rs79861172--A9.18%
rs9611486--28.99%
rs988257--A27.03%

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: 4/33 SNP entries detected (12%).

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

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