Traits - Genetic associations studied in mood-variability research

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Genetic associations studied in mood-variability research

General

Mood swings research studies inherited differences in how often and how strongly mood changes during everyday life.

GWAS work has identified variants linked to self-reported mood swings, with overlap with neuroticism and depression-related traits.

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

Sleep, stress, hormones, life events, relationships, mental health, and overall well-being strongly shape mood swings in practice.

Selected sample
Demo Report
Report markers
69 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
rs11712223CTT39.09%
rs6103271GGG17.28%
rs613872GTT16.90%
rs10188070GG34.94%
rs1563304CTT17.25%
rs28655666AAA45.57%
rs9671386GAA25.62%
rs11039149AGG26.95%
rs7202252CCC26.66%
rs11509880--A34.42%
rs11687833--T39.41%
rs11690710--34.18%
rs11877496--T49.66%
rs12137936--G30.71%
rs12524535--G6.90%
rs1261114--A38.03%
rs1360379--T39.56%
rs1440476--G39.33%
rs17487484--49.70%
rs1833070--A36.12%
rs1890408--T12.11%
rs1962104--44.96%
rs2503775--G13.11%
rs2678897--A38.86%
rs34160346--44.01%
rs34759087--T11.78%
rs35789697--A35.82%
rs35906288--29.80%
rs4578918--25.68%
rs4651205--T28.02%
rs4836789--C40.29%
rs56318386--T21.52%
rs56403421--32.70%
rs600011--C29.22%
rs67447472--T10.42%
rs68152875--A38.99%
rs6889822--38.57%
rs6895295--T22.37%
rs784256--A18.50%
rs7895261--G29.00%
rs9344688--G35.18%
rs9353806--A29.10%
rs9852417--A40.15%
rs10959813--A21.09%
rs10983783--T44.67%
rs11184994--T30.85%
rs12896360--32.01%
rs1373921--23.03%
rs1427027--T26.90%
rs17665188--21.39%
rs1881193--21.74%
rs199441--21.75%
rs241036--C21.71%
rs297346--36.61%
rs55657917--G21.34%
rs56059702--T44.33%
rs5758268--28.89%
rs79857651--A21.56%
rs8002014--A25.53%
rs9611567--G24.15%
rs9929242--A47.12%
rs11039409--C28.93%
rs11082011--T34.40%
rs11090039--A28.33%
rs112333322--G21.50%
rs12420205--T32.25%
rs7104036--38.66%
rs7107356--49.50%
rs72995548--T6.22%

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: 9/69 SNP entries detected (13%).

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

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