Genetic variant
rs9349379
rs9349379 is a single-letter difference in human DNA, on chromosome 6. Carrying it does not, on its own, mean you have or will develop any condition.
What is this?
Your DNA is a long sequence of four letters. At a few million positions, people commonly differ by a single letter; each of those positions is called a SNP (“snip”), and rs9349379 is the catalogue number of one of them. Which letters you carry there — one copy from each parent — is your genotype.
We hold only the basic reference record for this variant: its ID and position. Many catalogued variants have never been linked to anything.
Why might it matter?
ClinVar holds no clinical classification for this variant. That is the usual case: most catalogued variants have no known effect on health.
Do I have this variant?
If you have taken a consumer DNA test (23andMe, AncestryDNA and similar), you can download its raw data file and check. Create a free account, upload the file, and this page will show the letters you carry at rs9349379, if your test read this position.
Connect this with your blood results
A gene is a fixed instruction; a blood test shows what your body is doing now. CheckMyBloods reads the two side by side, so a variant can be set against the markers it could plausibly affect.
Blood markers do not diagnose a genetic condition, and a variant does not explain a blood result on its own. Together, with symptoms and family history, they give a clinician context.
What should I do next?
- Find out whether you carry it. Reading about a variant says nothing about you until you know your genotype.
- Put it in context. Add your blood results, so the variant can be read against what your body is doing.
- Ask questions. Dr. Hemsworth, our AI assistant, can explain this variant and your results in plain English.
- Take anything that worries you to a professional. A GP or genetic counsellor can order a confirmatory test and interpret it with your history.
This page is general information drawn from public research databases. It cannot diagnose anything, and it is not a substitute for advice from a doctor or genetic counsellor who knows your history.
Technical details
- dbSNP ID
- rs9349379
- Position
- chr6:12903725
Genome-wide association studies (20)
| Trait | Risk allele | OR / beta | P-value | Study |
|---|---|---|---|---|
| Coronary artery disease | A | OR 0.89 | 4E-114 | PubMed |
| Coronary artery disease | — | OR 0.11 | 4E-104 | PubMed |
| Coronary atherosclerosis (PheCode 411.4) | A | β 0.094 | 2E-96 | PubMed |
| Ischemic heart disease (PheCode 411) | A | β 0.084 | 7E-82 | PubMed |
| Coronary artery disease | A | OR 0.12 | 3E-77 | PubMed |
| Coronary artery disease | A | OR 0.12 | 3E-77 | PubMed |
| Coronary artery disease | A | OR 0.11 | 3E-76 | PubMed |
| Other chronic ischemic heart disease, unspecified (PheCode 411.8) | A | β 0.098 | 5E-73 | PubMed |
| Myocardial infarction | G | OR 0.15 | 4E-63 | PubMed |
| Myocardial infarction | G | OR 1.13 | 2E-60 | PubMed |
| Coronary atherosclerosis (PheCode 411.4) | A | β 0.094 | 5E-59 | PubMed |
| Myocardial infarction | — | OR 0.89 | 2E-55 | PubMed |
| Ischemic heart disease (PheCode 411) | A | β 0.083 | 2E-49 | PubMed |
| Other chronic ischemic heart disease, unspecified (PheCode 411.8) | A | β 0.098 | 2E-48 | PubMed |
| Migraine | A | OR 1.08 | 1E-47 | PubMed |
| Coronary artery disease (MTAG) | G | β 0.045 | 1E-47 | PubMed |
| Coronary artery / coronary heart disease (including heart attack, angina) | A | β 0.094 | 3E-47 | PubMed |
| Pulse pressure | G | OR 0.25 | 2E-44 | PubMed |
| Coronary artery disease | G | OR 1.14 | 2E-42 | PubMed |
| Takes medication for coronary artery/ coronary heart disease? | A | β 0.095 | 7E-42 | PubMed |
Sources
- dbSNP: rs9349379 — the reference record
- ClinVar — clinical interpretations submitted by laboratories
- SNPedia — community-written summaries
- GWAS Catalog — association studies