rs17465637
MIA3rs17465637 is a single-nucleotide polymorphism (SNP) in the MIA3 gene. Genespiral reads it in the Health & Wellness analysis to describe Heart Disease Risk.
- Gene
- MIA3
- Alleles
- A / G
- Genotypes
- AA, AG, GG
- Traits
- 1 trait across 1 analysis
An rsID such as rs17465637 is the reference number dbSNP assigns to one position in the genome where people commonly differ by a single letter. Raw data exports from 23andMe and AncestryDNA list your two alleles at that position as a genotype - for this marker one of AA, AG, GG. The order of the two letters carries no meaning, so AG and its reverse are the same genotype.
Alleles on this page are written on the forward (plus) strand, matching how consumer raw files report them. Other references sometimes describe the same variant on the opposite strand, which swaps A↔T and C↔G - see why the same variant can look different. The associations below are educational summaries of published research; they are not diagnoses, and the effect of any single SNP is usually modest.
Heart Disease Risk
Cardiovascular Health · Part of the Health & Wellness analysis
Linked to cholesterol and cardiovascular health.
| Genotype | Association |
|---|---|
| AA | Increased Risk |
| AG | Moderate Risk |
| GG | Lower Risk |
- Summary
- Specific gene variations impact cardiovascular disease risk.
- Scientific insights
- 'AA' alleles show increased risk, while 'GG' carriers tend to have lower susceptibility.
- Lifestyle tips
- Maintain a heart-healthy diet and monitor blood pressure regularly.
Check your genotype at rs17465637
Load your raw DNA file and Genespiral looks up rs17465637 along with every other marker in the Health & Wellness analysis. The file is parsed in your browser and never uploaded, so your genotype stays on your device.
- 1. Download your raw data from 23andMe or AncestryDNA.
- 2. Open the analysis below and choose the file.
- 3. Find Heart Disease Risk in your results.
Related
References
Primary databases for this variant. Use them to check allele orientation, population frequencies, and the underlying studies.
- dbSNP entry for rs17465637 - NCBI
- rs17465637 variant page - Ensembl
- rs17465637 summary - SNPedia
- Clinical significance records for rs17465637 - ClinVar
- MIA3 gene - NCBI Gene
Genespiral is an educational tool, not a medical service. Genetic associations describe tendencies observed across populations, not certainties for you. Read the full disclaimer.