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
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
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs1687482 | T G | T | G | 17.99% | Detected |
CADM2 GeneCards
cell adhesion molecule 2
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs74433724 | -- | A | G | 93.77% | No Data |
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
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs200580547 | -- | CAT | C | 86.87% | No Data |
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
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs12047316 | -- | T | C | 91.71% | No Data |
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
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs7328259 | -- | G | A | 40.17% | No Data |
LMF1 GeneCards
lipase maturation factor 1
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs56274719 | -- | C | A | 77.89% | No Data |
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
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs34577613 | -- | C | T | 89.99% | No Data |
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
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs2025251 | -- | T | G | 42.72% | No Data |
NKAIN3 GeneCards
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs16928927 | -- | C | T | 93.49% | No Data |
SRGAP3 GeneCards
SLIT-ROBO Rho GTPase activating protein 3
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs201599726 | -- | TACACATACATAC | T | 21.10% | No Data |
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 |
|---|---|---|---|---|
| rs1687482 | 3 | TG | G | 17.99% |
| rs9847523 | 3 | GA | A | 70.19% |
| rs61323942 | 14 | AC | C | 67.86% |
| rs12047316 | 1 | -- | C | 91.71% |
| rs34577613 | 2 | -- | T | 89.99% |
| rs74433724 | 3 | -- | G | 93.77% |
| rs6764777 | 3 | -- | G | 17.95% |
| rs201599726 | 3 | -- | T | 21.10% |
| rs9862276 | 3 | -- | T | 91.51% |
| rs200580547 | 4 | -- | C | 86.87% |
| rs34361130 | 4 | -- | T | 84.58% |
| rs2025251 | 6 | -- | G | 42.72% |
| rs16928927 | 8 | -- | T | 93.49% |
| rs7328259 | 13 | -- | A | 40.17% |
| rs68110513 | 13 | -- | A | 67.74% |
| rs7986060 | 13 | -- | A | 68.78% |
| rs2329317 | 13 | -- | A | 59.09% |
| rs56274719 | 16 | -- | A | 77.89% |
| rs17663182 | 18 | -- | T | 92.27% |
The following peer-reviewed scientific studies support the genetic associations analyzed in this report.
What's Next?
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