Genetic variant
rs11153730
rs11153730 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 rs11153730 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 rs11153730, 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
- rs11153730
- Position
- chr6:118346359
Genome-wide association studies (20)
| Trait | Risk allele | OR / beta | P-value | Study |
|---|---|---|---|---|
| QT interval | T | β 0.096 | 6E-246 | PubMed |
| QRS duration | T | β 0.064 | 4E-109 | PubMed |
| JT interval | T | β 0.062 | 2E-104 | PubMed |
| Pulse rate (UKB data field 102) | C | β 0.041 | 1E-94 | PubMed |
| QT interval | C | OR 1.41 | 5E-74 | PubMed |
| ECG cardiac MRI latent space | — | — | 4E-71 | PubMed |
| QRS duration | C | OR 0.58 | 1E-70 | PubMed |
| QT interval | T | OR 1.65 | 2E-67 | PubMed |
| ECG latent space | — | — | 1E-65 | PubMed |
| PR interval | T | OR 1 | 3E-54 | PubMed |
| QRS duration | C | OR 0.58 | 9E-38 | PubMed |
| Electrocardiogram morphology (amplitude at temporal datapoints) | T | β 0.07 | 4E-37 | PubMed |
| QT interval | C | OR 2.25 | 2E-35 | PubMed |
| QTc interval | — | OR 1.34 | 5E-32 | PubMed |
| QT interval | C | β 0.09 | 2E-29 | PubMed |
| QRS duration | — | OR 0.63 | 7E-29 | PubMed |
| QT interval | T | β 0.064 | 6E-28 | PubMed |
| QT interval | T | β 0.06 | 3E-24 | PubMed |
| Heart rate | T | OR 0.38 | 8E-21 | PubMed |
| QRS duration | T | OR 0.54 | 5E-19 | PubMed |
Sources
- dbSNP: rs11153730 — the reference record
- ClinVar — clinical interpretations submitted by laboratories
- SNPedia — community-written summaries
- GWAS Catalog — association studies