Genetic Predisposition

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

Your Result

Lower Rapid automised naming of letters performance 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
12 genes analyzed 1 with detected variants
Variant Detected

UROC1 GeneCards

This gene encodes an enzyme involved in the second step of histidine catabolism, metabolizing urocanic acid to formiminoglutamic acid. Deficiency of this enzyme results in urocanic aciduria, and is an apparent cause of mental retardation. Multiple transcript variants encoding different isoforms have been found for this gene.

Genomic Location
Chr 3 Start: 126,200,009 End: 126,236,616 Build: HG19
Associated SNPs
1 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

CADM2 GeneCards

cell adhesion molecule 2

Genomic Location
Chr 3 Start: 85,008,140 End: 86,123,579 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ELMOD2 GeneCards

This gene encodes one of six engulfment and motility (ELMO) domain-containing proteins. This gene is thought to play a role in antiviral responses. Mutations in this gene may be involved in the cause of familial idiopathic pulmonary fibrosis.

Genomic Location
Chr 4 Start: 141,445,322 End: 141,474,924 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

FGF14-IT1 GeneCards

Genomic Location
Chr 13 Start: 102,944,670 End: 103,046,869 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

FMN2 GeneCards

This gene is a member of the formin homology protein family. The encoded protein is thought to have essential roles in organization of the actin cytoskeleton and in cell polarity. This protein mediates the formation of an actin mesh that positions the spindle during oogenesis and also regulates the formation of actin filaments in the nucleus. This protein also forms a perinuclear actin/focal-adhesion system that regulates the shape and position of the nucleus during cell migration. Mutations in this gene have been associated with infertility and also with an autosomal recessive form of intellectual disability (MRT47). Alternatively spliced transcript variants have been identified.

Genomic Location
Chr 1 Start: 240,255,183 End: 240,638,487 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

GPC5 GeneCards

Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation.

Genomic Location
Chr 13 Start: 92,050,875 End: 93,519,490 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

LMF1 GeneCards

lipase maturation factor 1

Genomic Location
Chr 16 Start: 903,634 End: 1,031,613 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

MYRIP GeneCards

myosin VIIA and Rab interacting protein

Genomic Location
Chr 3 Start: 39,850,405 End: 40,301,812 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

NEB GeneCards

This gene encodes nebulin, a giant protein component of the cytoskeletal matrix that coexists with the thick and thin filaments within the sarcomeres of skeletal muscle. In most vertebrates, nebulin accounts for 3 to 4% of the total myofibrillar protein. The encoded protein contains approximately 30-amino acid long modules that can be classified into 7 types and other repeated modules. Protein isoform sizes vary from 600 to 800 kD due to alternative splicing that is tissue-, species-,and developmental stage-specific. Of the 183 exons in the nebulin gene, at least 43 are alternatively spliced, although exons 143 and 144 are not found in the same transcript. Of the several thousand transcript variants predicted for nebulin, the RefSeq Project has decided to create three representative RefSeq records. Mutations in this gene are associated with recessive nemaline myopathy.

Genomic Location
Chr 2 Start: 152,341,853 End: 152,591,001 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

NKAIN2 GeneCards

This gene encodes a transmembrane protein that interacts with the beta subunit of a sodium/potassium-transporting ATPase. A chromosomal translocation involving this gene is a cause of lymphoma. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Genomic Location
Chr 6 Start: 124,125,010 End: 125,146,786 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Genomic Location
Chr 8 Start: 63,161,413 End: 63,912,211 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

SRGAP3 GeneCards

SLIT-ROBO Rho GTPase activating protein 3

Genomic Location
Chr 3 Start: 9,022,275 End: 9,291,330 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

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Coverage: 3/19 SNPs detected (15%)
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.