Genetic Predisposition
Based on your genetic markers, your predisposition to this trait is shown below
Your Result
Lower Anxiety susceptibility predisposition
Was this result accurate for you?
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
CADM2 GeneCards
cell adhesion molecule 2
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs9829032 | G G | A | G | 38.10% | Detected |
| rs76508707 | -- | C | T | 45.33% | No Data |
| rs4856278 | -- | A | G | 83.25% | No Data |
| rs9828679 | -- | T | C | 11.28% | No Data |
| rs7652808 | -- | T | G | 75.74% | No Data |
DPYD GeneCards
The protein encoded by this gene is a pyrimidine catabolic enzyme and the initial and rate-limiting factor in the pathway of uracil and thymidine catabolism. Mutations in this gene result in dihydropyrimidine dehydrogenase deficiency, an error in pyrimidine metabolism associated with thymine-uraciluria and an increased risk of toxicity in cancer patients receiving 5-fluorouracil chemotherapy. Two transcript variants encoding different isoforms have been found for this gene.
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs7526108 | A A | G | A | 76.46% | Detected |
BDNF-AS GeneCards
BDNF antisense RNA
Genomic Location
No SNPs found for this gene in your DNA data.
CNNM2 GeneCards
This gene encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play an important role in magnesium homeostasis by mediating the epithelial transport and renal reabsorption of Mg2+. Mutations in this gene are associated with renal hypomagnesemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs3902934 | -- | A | G | 42.43% | No Data |
ITIH4 GeneCards
The protein encoded by this gene is secreted into the blood, where it is cleaved by plasma kallikrein into two smaller forms. Expression of this gene has been detected only in liver, and it seems to be upregulated during surgical trauma. This gene is part of a cluster of similar genes on chromosome 3. Two transcript variants encoding different isoforms have been found for this gene.
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs2071044 | -- | C | T | 55.27% | No Data |
LINC00678 GeneCards
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs11030088 | -- | G | A | 12.30% | No Data |
PINX1 GeneCards
PIN2 (TERF1) interacting telomerase inhibitor 1
Genomic Location
No SNPs found for this gene in your DNA data.
SOX7 GeneCards
This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. The protein may play a role in tumorigenesis. A similar protein in mice is involved in the regulation of the wingless-type MMTV integration site family (Wnt) pathway.
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs28570522 | -- | A | G | 60.74% | 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 |
|---|---|---|---|---|
| rs7526108 | 1 | AA | A | 76.46% |
| rs4129585 | CC | C | 76.12% | |
| rs9829032 | 3 | GG | G | 38.10% |
| rs2672852 | 2 | -- | T | 54.39% |
| rs10174328 | 2 | -- | T | 27.42% |
| rs77165542 | 2 | -- | T | 1.04% |
| rs2071044 | 3 | -- | T | 55.27% |
| rs76508707 | 3 | -- | T | 45.33% |
| rs4856278 | 3 | -- | G | 83.25% |
| rs9828679 | 3 | -- | C | 11.28% |
| rs7652808 | 3 | -- | G | 75.74% |
| rs10027492 | 4 | -- | T | 57.65% |
| rs2458604 | 4 | -- | A | 40.02% |
| rs3800227 | 6 | -- | G | 53.10% |
| rs28570522 | 8 | -- | G | 60.74% |
| rs3902934 | 10 | -- | G | 42.43% |
| rs11030088 | 11 | -- | A | 12.30% |
| rs3764002 | 12 | -- | T | 25.70% |
| rs8054556 | 16 | -- | A | 39.46% |
| rs17175643 | 18 | -- | T | 21.11% |
The following peer-reviewed scientific studies support the genetic associations analyzed in this report.
What's Next?
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