Genetic Predisposition
Based on your genetic markers, your predisposition to this trait is shown below
Your Result
Lower Sleep Duration 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
MACROD2 GeneCards
The protein encoded by this gene is a deacetylase involved in removing ADP-ribose from mono-ADP-ribosylated proteins. The encoded protein has been shown to translocate from the nucleus to the cytoplasm upon DNA damage.
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs6034146 | A C | A | C | 51.38% | Detected |
ASCL4 GeneCards
Genomic Location
No SNPs found for this gene in your DNA data.
C2orf69 GeneCards
chromosome 2 open reading frame 69
Genomic Location
No SNPs found for this gene in your DNA data.
CBY1 GeneCards
Beta-catenin is a transcriptional activator and oncoprotein involved in the development of several cancers. The protein encoded by this gene interacts directly with the C-terminal region of beta-catenin, inhibiting oncogenic beta-catenin-mediated transcriptional activation by competing with transcription factors for binding to beta-catenin. Two transcript variants encoding different isoforms have been found for this gene.
Genomic Location
No SNPs found for this gene in your DNA data.
DDX17 GeneCards
DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and splicesosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is an ATPase activated by a variety of RNA species, but not by dsDNA. This protein, and that encoded by DDX5 gene, are more closely related to each other than to any other member of the DEAD box family. This gene can encode multiple isoforms due to both alternative splicing and the use of alternative translation initiation codons, including a non-AUG (CUG) start codon.
Genomic Location
No SNPs found for this gene in your DNA data.
DMC1 GeneCards
This gene encodes a member of the superfamily of recombinases (also called DNA strand-exchange proteins). Recombinases are important for repairing double-strand DNA breaks during mitosis and meiosis. This protein, which is evolutionarily conserved, is reported to be essential for meiotic homologous recombination and may thus play an important role in generating diversity of genetic information. Alternative splicing results in multiple transcript variants.
Genomic Location
No SNPs found for this gene in your DNA data.
JOSD1 GeneCards
Josephin domain containing 1
Genomic Location
No SNPs found for this gene in your DNA data.
KDELR3 GeneCards
KDEL endoplasmic reticulum protein retention receptor 3
Genomic Location
No SNPs found for this gene in your DNA data.
MAIP1 GeneCards
Genomic Location
No SNPs found for this gene in your DNA data.
PRDM4 GeneCards
Genomic Location
No SNPs found for this gene in your DNA data.
SPATS2L GeneCards
spermatogenesis associated serine rich 2 like
Genomic Location
No SNPs found for this gene in your DNA data.
SUN2 GeneCards
Sad1 and UNC84 domain containing 2
Genomic Location
No SNPs found for this gene in your DNA data.
TOMM22 GeneCards
Genomic Location
No SNPs found for this gene in your DNA data.
TYW5 GeneCards
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs12470989 | -- | A | G | 18.23% | No Data |
WSCD2 GeneCards
WSC domain containing 2
Genomic Location
No SNPs found for this gene in your DNA 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 |
|---|---|---|---|---|
| rs7616632 | 3 | TG | G | 34.68% |
| rs7644809 | 3 | CC | C | 31.03% |
| rs7915425 | 10 | CC | C | 89.60% |
| rs1263056 | 11 | AG | G | 68.05% |
| rs4402351 | 12 | AG | G | 25.40% |
| rs3095508 | 16 | CA | A | 42.55% |
| rs9903973 | 17 | TT | T | 72.08% |
| rs6034146 | 20 | AC | C | 51.38% |
| rs2235229 | 22 | CT | T | 48.12% |
| rs269054 | 1 | -- | A | 32.13% |
| rs61796569 | 1 | -- | T | 23.16% |
| rs12567114 | 1 | -- | A | 26.12% |
| rs915416 | 1 | -- | G | 67.91% |
| rs62120041 | 2 | -- | C | 2.88% |
| rs10173260 | 2 | -- | C | 51.28% |
| rs11885663 | 2 | -- | T | 17.57% |
| rs12470989 | 2 | -- | G | 18.23% |
| rs7556815 | 2 | -- | A | 18.11% |
| rs4538155 | 2 | -- | T | 53.75% |
| rs374153 | 2 | -- | T | 81.47% |
| rs4128364 | 2 | -- | C | 38.00% |
| rs75539574 | 2 | -- | C | 2.76% |
| rs12611523 | 2 | -- | G | 54.19% |
| rs17732997 | 3 | -- | G | 39.20% |
| rs13088093 | 3 | -- | G | 27.68% |
| rs2192528 | 4 | -- | G | 66.63% |
| rs35531607 | 4 | -- | C | 47.90% |
| rs17427571 | 4 | -- | G | 26.70% |
| rs13109404 | 4 | -- | G | 1.74% |
| rs56372231 | 5 | -- | T | 30.53% |
| rs460692 | 5 | -- | T | 89.76% |
| rs180769 | 5 | -- | C | 68.69% |
| rs151014368 | 5 | -- | A | 10.48% |
| rs365663 | 5 | -- | G | 61.46% |
| rs11567976 | 5 | -- | T | 42.71% |
| rs9345234 | 6 | -- | C | 42.37% |
| rs9382445 | 6 | -- | C | 43.73% |
| rs34556183 | 6 | -- | G | 25.00% |
| rs113113059 | 6 | -- | C | 40.62% |
| rs2231265 | 6 | -- | G | 85.40% |
| rs34731055 | 7 | -- | T | 16.43% |
| rs7806045 | 7 | -- | C | 20.71% |
| rs330088 | 8 | -- | C | 63.44% |
| rs73219758 | 8 | -- | A | 13.48% |
| rs1776776 | 9 | -- | C | 19.67% |
| rs10973207 | 9 | -- | T | 10.96% |
| rs10761674 | 10 | -- | T | 43.19% |
| rs12246842 | 10 | -- | G | 60.44% |
| rs11190970 | 10 | -- | A | 9.19% |
| rs4592416 | 11 | -- | G | 39.70% |
| rs1517572 | 11 | -- | C | 43.19% |
| rs174560 | 11 | -- | C | 32.63% |
| rs12791153 | 11 | -- | T | 4.17% |
| rs1939455 | 11 | -- | T | 14.58% |
| rs1553132 | 11 | -- | G | 23.04% |
| rs11602180 | 11 | -- | T | 25.38% |
| rs1057703 | 11 | -- | G | 22.10% |
| rs4767550 | 12 | -- | G | 33.65% |
| rs11614986 | 12 | -- | G | 15.95% |
| rs34354917 | 12 | -- | A | 11.92% |
| rs61985058 | 14 | -- | T | 5.81% |
| rs55658675 | 14 | -- | T | 20.83% |
| rs10483350 | 14 | -- | G | 16.73% |
| rs11621908 | 14 | -- | T | 9.90% |
| rs6575005 | 14 | -- | C | 33.71% |
| rs8038326 | 15 | -- | G | 12.28% |
| rs11643715 | 16 | -- | G | 27.12% |
| rs8050478 | 16 | -- | A | 44.37% |
| rs205024 | 17 | -- | T | 33.27% |
| rs7503199 | 17 | -- | T | 23.54% |
| rs10421649 | 19 | -- | A | 44.19% |
| rs2072727 | 20 | -- | C | 54.13% |
The following peer-reviewed scientific studies support the genetic associations analyzed in this report.
What's Next?
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