Genetic Predisposition

Based on your genetic markers, your predisposition to this trait is shown below

Your Result

Lower Post-traumatic stress disorder predisposition

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Scientific Evidence

Understanding the Data
  • SNP: A specific genetic marker relevant to this trait (e.g., rs2588978)
  • Genotype: Your genetic makeup at the given SNP location (e.g., CC)
  • Variant allele: The alternative DNA sequence at the SNP site
  • Variant allele frequency: Percentage of population carrying this variant
  • Variant found: Whether the variant was detected in your DNA file
6 genes analyzed 1 with detected variants
Variant Detected

POGK GeneCards

pogo transposable element derived with KRAB domain

Genomic Location
Chr 1 Start: 166,808,712 End: 166,825,596 Build: HG19
Associated SNPs
1 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

CSMD1 GeneCards

CUB and Sushi multiple domains 1

Genomic Location
Chr 8 Start: 2,792,883 End: 4,852,436 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

LGR6 GeneCards

leucine rich repeat containing G protein-coupled receptor 6

Genomic Location
Chr 1 Start: 202,162,927 End: 202,288,889 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

LHX2 GeneCards

LIM homeobox 2

Genomic Location
Chr 9 Start: 126,774,047 End: 126,795,580 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

PRTFDC1 GeneCards

phosphoribosyl transferase domain containing 1

Genomic Location
Chr 10 Start: 25,137,543 End: 25,241,535 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

UST GeneCards

uronyl 2-sulfotransferase

Genomic Location
Chr 6 Start: 149,068,166 End: 149,398,126 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

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Coverage: 1/7 SNPs detected (14%)
Reference: Human Genome Build 37 (HG19)
Generated: March 02, 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.