Traits - Genetic associations studied in religious-attendance research

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Genetic associations studied in religious-attendance research

Personality Traits

This trait reflects research on inherited factors associated with frequent attendance at a religious group, used in large UK Biobank-style studies.

GWAS work has identified some variants linked to this behavior, often overlapping with personality and social traits.

This result reflects research-level variation in social behavior and is not a value judgment about religious participation.

Family upbringing, culture, life events, and personal beliefs strongly shape this behavior.

Selected sample
Demo Report
Report markers
19 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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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
rs1991083CT31.95%
rs6545977GAA51.60%
rs10085831--78.11%
rs1031831--66.82%
rs1160543--59.71%
rs12156017--G35.17%
rs12197025--G81.28%
rs13082569--A64.79%
rs1422192--84.27%
rs2726478--A58.30%
rs332828--54.19%
rs3747630--A75.77%
rs4729379--G31.60%
rs62085660--G25.76%
rs6722794--58.44%
rs6862251--69.90%
rs699534--42.70%
rs7998050--29.70%
rs9837520--A72.16%

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: 2/19 SNP entries detected (10%).

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

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SAMPLE REPORT Example DNA profile This is a sample report with example data. It is not your personal report, and the results do not describe you.
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