Navigating the SNP & gene pages
Your SNP and gene pages show the genotypes you have for different genetic variants called SNPs (Single Nucleotide Polymorphisms). This article explains how to read those pages.
Understanding your SNP table
Each column in your SNP table gives you important information:
| Column | What it means |
|---|---|
| Variant (SNP) | A tiny change in your DNA. Pronounced "snips," these are Single Nucleotide Polymorphisms. Watch this video to learn more about SNPs. |
| Genotype | The specific alleles (variants) you carry for this SNP. |
| Frequency | Also called allele frequency. Shows how common this allele is in a population, based on the ethnicity you selected when signing up. |
| Alternative Allele | The allele that differs from the reference sequence. Learn more about alternative alleles. |
| Impact | A score showing how strongly this SNP affects the gene. Higher scores indicate greater impact. |
Understanding the icons on your pages
Icons on your SNP and gene pages give you helpful context about your results:
- âšī¸ Informational tooltip (small "i" in a circle): Provides general information about insertions and deletions (INDELs). This appears for everyone and does not mean you personally have that INDEL.
- đŖ Human icon (purple-filled with human symbol): Specific to your results. This appears next to the alleles you carry, highlighting variations in your genetic data.
These icons help you distinguish between general genetic information and your personal genetic insights, making your results easier to interpret accurately.
Learn more
For more on genetic concepts, explore:
Looking for help with your results?
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- AI Hyperintelligence â your built-in AI health coach, available right in your account.
- Connect via MCP integration â link your SelfDecode data to ChatGPT or Claude for AI-powered insights using your own account.
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