Genetic Predisposition

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

Your Result

Lower Sleep Quality 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
5 genes analyzed 3 with detected variants
Variant Detected

AC007686.1 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
1 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Variant Detected

CACNA1C GeneCards

This gene encodes an alpha-1 subunit of a voltage-dependent calcium channel. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization. The alpha-1 subunit consists of 24 transmembrane segments and forms the pore through which ions pass into the cell. The calcium channel consists of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. There are multiple isoforms of each of these proteins, either encoded by different genes or the result of alternative splicing of transcripts. The protein encoded by this gene binds to and is inhibited by dihydropyridine. Alternative splicing results in many transcript variants encoding different proteins. Some of the predicted proteins may not produce functional ion channel subunits.

Genomic Location
Chr 12 Start: 2,162,153 End: 2,807,116 Build: HG19
Associated SNPs
1 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Variant Detected

SLC2A13 GeneCards

Genomic Location
Chr 12 Start: 40,148,827 End: 40,499,883 Build: HG19
Associated SNPs
1 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

FGF12 GeneCards

The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This growth factor lacks the N-terminal signal sequence present in most of the FGF family members, but it contains clusters of basic residues that have been demonstrated to act as a nuclear localization signal. When transfected into mammalian cells, this protein accumulated in the nucleus, but was not secreted. The specific function of this gene has not yet been determined.

Genomic Location
Chr 3 Start: 191,857,179 End: 192,445,330 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Genomic Location
Chr 9 Start: 25,676,967 End: 25,678,442 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

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Coverage: 3/7 SNPs detected (42%)
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.