Genetic variant
rs1815739
rs1815739 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 rs1815739 is the catalogue number of one of them. Which letters you carry there — one copy from each parent — is your genotype.
This SNP, in the ACTN3 gene, encodes a premature stop codon in a muscle protein called alpha-actinin...
From SNPedia
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 rs1815739, 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
- rs1815739
- Position
- chr11:66560624
Genome-wide association studies (8)
| Trait | Risk allele | OR / beta | P-value | Study |
|---|---|---|---|---|
| MSTN/RGMA protein level ratio | — | β 0.09 | 1E-43 | PubMed |
| Body composition (MOSTest) | — | OR 11.13 | 9E-29 | PubMed |
| MSTN protein levels | C | β 0.051 | 2E-25 | PubMed |
| MYBPC2 protein levels | C | β 0.044 | 2E-13 | PubMed |
| Insomnia | T | β 0.007 | 6E-13 | PubMed |
| Growth/differentiation factor 11/8 levels (GDF11.MSTN.2765.4.3) | C | OR 0.17 | 8E-12 | PubMed |
| Estimated glomerular filtration rate (creatinine) | C | OR 5.89 | 4E-9 | PubMed |
| Sleep apnea (MTAG) | — | β 0.019 | 2E-8 | PubMed |
Sources
- dbSNP: rs1815739 — the reference record
- ClinVar — clinical interpretations submitted by laboratories
- SNPedia — community-written summaries
- GWAS Catalog — association studies