Genetic variant
rs11191580
rs11191580 is a single-letter difference in human DNA, on chromosome 10. 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 rs11191580 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 rs11191580, 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
- rs11191580
- Position
- chr10:103146454
Genome-wide association studies (20)
| Trait | Risk allele | OR / beta | P-value | Study |
|---|---|---|---|---|
| Systolic blood pressure | C | OR 0.97 | 1E-111 | PubMed |
| Systolic blood pressure (MTAG) | C | β 0.06 | 4E-83 | PubMed |
| Pulse pressure | C | OR 0.56 | 3E-74 | PubMed |
| Systolic blood pressure | — | — | 4E-57 | PubMed |
| Diastolic blood pressure (MTAG) | C | β 0.048 | 9E-56 | PubMed |
| Diastolic blood pressure | C | OR 0.42 | 2E-55 | PubMed |
| Systolic blood pressure | T | β 0.05 | 7E-33 | PubMed |
| Systolic blood pressure (UKB data field 4080) | C | β 0.041 | 2E-31 | PubMed |
| Systolic blood pressure | T | β 0.06 | 1E-23 | PubMed |
| Hypertension | C | β 0.084 | 9E-21 | PubMed |
| Hypertension | — | OR 0.11 | 3E-20 | PubMed |
| Cardiovascular disease | — | — | 2E-19 | PubMed |
| Pallidum iron levels (R2* MRI) | T | OR 0.1 | 6E-16 | PubMed |
| Pulse pressure | T | β 0.03 | 1E-15 | PubMed |
| Systolic blood pressure (long-term average) | T | OR 0.97 | 4E-15 | PubMed |
| Diastolic blood pressure (UKB data field 4079) | C | β 0.029 | 5E-15 | PubMed |
| Systolic blood pressure | T | OR 0.67 | 7E-15 | PubMed |
| Hypertension | T | OR 0.11 | 2E-13 | PubMed |
| Pulse pressure | T | OR 0.43 | 9E-13 | PubMed |
| Body mass index | T | β 0.031 | 2E-11 | PubMed |
Sources
- dbSNP: rs11191580 — the reference record
- ClinVar — clinical interpretations submitted by laboratories
- SNPedia — community-written summaries
- GWAS Catalog — association studies