Genetic variant
rs964184
rs964184 is a single-letter difference in human DNA, on chromosome 11. 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 rs964184 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 rs964184, 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
- rs964184
- Position
- chr11:116778201
Genome-wide association studies (20)
| Trait | Risk allele | OR / beta | P-value | Study |
|---|---|---|---|---|
| Triglyceride levels | — | — | 1E-3751 | PubMed |
| Triglyceride levels | C | OR 0.25 | 3E-2157 | PubMed |
| Triglycerides in small VLDL | C | OR 0.25 | 5E-1608 | PubMed |
| Triglycerides in small HDL | C | OR 0.24 | 3E-1586 | PubMed |
| Triglycerides to Total Lipids in Small HDL percentage | C | OR 0.23 | 1E-1505 | PubMed |
| Free Cholesterol to Total Lipids in Small LDL percentage | C | OR 0.23 | 8E-1498 | PubMed |
| Triglycerides | C | OR 0.22 | 1E-1483 | PubMed |
| Free Cholesterol to Total Lipids in Medium LDL percentage | C | OR 0.23 | 7E-1482 | PubMed |
| Triglycerides in HDL | C | OR 0.23 | 7E-1455 | PubMed |
| Triglycerides to Total Lipids in Medium HDL percentage | C | OR 0.23 | 1E-1444 | PubMed |
| Triglycerides to Total Lipids in Very Large HDL percentage | C | OR 0.22 | 2E-1428 | PubMed |
| Triglycerides to Total Lipids in Large HDL percentage | C | OR 0.22 | 5E-1389 | PubMed |
| Triglycerides in medium HDL | C | OR 0.23 | 7E-1355 | PubMed |
| Average diameter for VLDL particles | C | OR 0.21 | 1E-1285 | PubMed |
| Triglyceride to phosphoglyceride ratio | C | OR 0.21 | 1E-1282 | PubMed |
| Triglycerides in very small VLDL | C | OR 0.22 | 6E-1281 | PubMed |
| Total triglycerides levels | C | OR 0.22 | 9E-1268 | PubMed |
| Free Cholesterol to Total Lipids in Large LDL percentage | C | OR 0.21 | 6E-1257 | PubMed |
| Triglycerides in small LDL | C | OR 0.22 | 1E-1239 | PubMed |
| Triglycerides in VLDL | C | OR 0.21 | 3E-1211 | PubMed |
Sources
- dbSNP: rs964184 — the reference record
- ClinVar — clinical interpretations submitted by laboratories
- SNPedia — community-written summaries
- GWAS Catalog — association studies