What This Trait Studies

This section explains the population-level genetic research behind this trait. It is not an individual diagnosis or prediction.

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.

20 Genetic markers studied
3 Detected in your data
0 Genes analyzed
1 Research study

Not an individual prediction. This section summarizes population-level genetic research. It is not a personal diagnosis, a screening result, or a claim about you specifically. If this topic is a health, behavioral, or wellbeing concern for you, please talk with a qualified professional rather than relying on this genetic report.

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Scientific Evidence

These are the genetic markers (SNPs) analyzed for this trait. Variations detected in your genome are listed under the "Genotype" column. SNPs showing "--" were not identified in your DNA file.

SNP Chromosome Genotype Variant Allele Frequency
rs4129585 CC 23.88%
rs7526108 AA 23.54%
rs9829032 GG G 38.10%
rs10027492 -- 42.35%
rs11030088 -- A 12.30%
rs17175643 -- 78.89%
rs2458604 -- A 40.02%
rs28570522 -- 39.26%
rs3764002 -- T 25.70%
rs3800227 -- 46.91%
rs3902934 -- 57.57%
rs8054556 -- 60.54%
rs10174328 -- 72.58%
rs2071044 -- 44.73%
rs2672852 -- 45.61%
rs4856278 -- 16.75%
rs76508707 -- T 45.33%
rs7652808 -- 24.26%
rs77165542 -- 98.96%
rs9828679 -- C 11.28%
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.

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Coverage: 3/20 SNPs detected (15%)
Reference: Human Genome Build 37 (HG19)
Generated: September 23, 2026
DNA Genics reports genotypes based on the 'positive' strand of the human genome reference sequence. Other testing companies may report using the opposite strand, requiring conversion for accurate comparison.