Traits - Worry tendency

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Worry tendency

General

Worry research uses self-report scales to measure how often and how strongly people worry in everyday life.

GWAS work has identified variants linked to self-reported worry, with overlap with anxiety and neuroticism traits.

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

Sleep, stress, life events, mental health support, and current context strongly shape day-to-day worry.

Selected sample
Demo Report
Report markers
147 SNP entries
Genes
0
Research
1 study
Your report

Genetic association

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Higher worry 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
rs10005233TT33.19%
rs1572982AAA59.07%
rs1593304GG40.58%
rs17196295AGG10.40%
rs353547CC34.68%
rs1938386GTT56.93%
rs9671386GA26.68%
rs9811546GAA22.78%
rs1163085GAA63.90%
rs1248860GA44.73%
rs12938031GGG17.07%
rs2710323CCC52.18%
rs3026401CT35.68%
rs7152906TC65.81%
rs722599CCC41.43%
rs7355953TCC10.00%
rs888415GG45.77%
rs1017730GAA16.99%
rs10769256TTT35.96%
rs10871777AGG24.58%
rs1539844GAA8.65%
rs9829032AGG38.10%
rs9966951GAA32.71%
rs3740688TT36.08%
rs3897644CT49.22%
rs9870384CTT22.98%
rs10034259--C14.32%
rs13324323--T22.78%
rs150491901--A4.87%
rs28639817--G15.24%
rs332828--A35.46%
rs34644694--29.91%
rs391236--G19.29%
rs4405857--39.36%
rs4684833--20.31%
rs480330--T41.95%
rs483143--C12.60%
rs488359--G57.65%
rs502652--T19.73%
rs57360718--C8.03%
rs61731122--A0.90%
rs62253085--45.43%
rs62551581--C8.89%
rs7033345--C38.66%
rs7567451--T56.67%
rs78260322--G3.17%
rs79827531--A12.16%
rs998884--G38.98%
rs12188167--G6.77%
rs2488401--T23.64%
rs2672852--45.61%
rs1724725--2.04%
rs17532098--T5.03%
rs2236939--T11.16%
rs13262595--24.04%
rs2413631--A19.17%
rs2435210--T25.14%
rs246914--C12.46%
rs11663050--G45.67%
rs12145083--A16.21%
rs12260436--C35.54%
rs12484971--T25.16%
rs12765002--T28.17%
rs12923795--69.27%
rs12957516--53.25%
rs13094915--C55.05%
rs13282237--G60.22%
rs1330745--C11.00%
rs13328187--C14.48%
rs1368748--50.40%
rs28426374--T52.38%
rs3117425--T4.45%
rs3124377--40.12%
rs3742020--C33.65%
rs3751855--C47.96%
rs3988211--2.82%
rs4245150--19.61%
rs4752856--A25.72%
rs4799723--21.59%
rs4856278--16.75%
rs4937872--G60.94%
rs525773--A56.09%
rs55997507--42.53%
rs56084168--T16.49%
rs56133711--A11.34%
rs589092--52.10%
rs59735493--A43.55%
rs60642411--A24.94%
rs61734645--G1.96%
rs61991614--A14.24%
rs62064641--C8.69%
rs62081501--A5.41%
rs62081537--C17.01%
rs62096058--A33.57%
rs62250661--A40.83%
rs6445541--T33.75%
rs6478623--G36.14%
rs6807666--35.48%
rs6851494--31.35%
rs7023933--T28.85%
rs7207400--C26.30%
rs7220839--T41.05%
rs72893199--C15.81%
rs730356--A12.20%
rs75195552--A9.01%
rs75614054--T5.15%
rs76508707--T45.33%
rs77420391--A15.16%
rs77432625--G5.39%
rs80533--17.41%
rs8067056--C30.91%
rs818219--C58.71%
rs9936170--G45.55%
rs9861237--C34.86%
rs9836178--27.30%
rs10501320--C8.83%
rs10507274--C2.42%
rs10850379--T34.11%
rs11090045--A21.29%
rs11159097--C31.67%
rs11191392--A51.46%
rs11204421--C38.76%
rs112591851--T0.90%
rs1426371--A25.66%
rs1427041--25.06%
rs16902946--C0.00%
rs1826787--T22.98%
rs1890184--C42.31%
rs9854869--A11.22%
rs3213716--A31.15%
rs34011394--T28.85%
rs34135146--C4.53%
rs34569203--C9.66%
rs352140--58.45%
rs3740393--C21.03%
rs3740397--C35.02%
rs3785879--A46.77%
rs4434138--G34.13%
rs4526367--21.81%
rs4687552--C30.97%
rs2194027--A31.89%
rs1998122--A31.09%
rs9896243--G12.32%
rs1296171--G55.85%
rs2407746--G22.56%
rs9837462--A15.81%
rs9828595--G23.04%

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: 26/147 SNP entries detected (17%).

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

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