Genetic variant
rs1042579
rs1042579 is a single-letter difference in human DNA, on chromosome 20. 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 rs1042579 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 rs1042579, 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
- rs1042579
- Position
- chr20:23048087
Genome-wide association studies (12)
| Trait | Risk allele | OR / beta | P-value | Study |
|---|---|---|---|---|
| Thrombomodulin levels | A | OR 0.4 | 2E-318 | PubMed |
| IFNGR1/THBD protein level ratio | — | OR 0.29 | 2E-268 | PubMed |
| JAM2/THBD protein level ratio | — | OR 0.26 | 8E-195 | PubMed |
| ROR1/THBD protein level ratio | — | OR 0.24 | 7E-186 | PubMed |
| TGFBR2/THBD protein level ratio | — | OR 0.24 | 3E-183 | PubMed |
| IL18BP/THBD protein level ratio | — | OR 0.25 | 4E-180 | PubMed |
| HYOU1/THBD protein level ratio | — | OR 0.24 | 1E-178 | PubMed |
| CD46/THBD protein level ratio | — | OR 0.24 | 8E-175 | PubMed |
| THBD protein levels | A | OR 0.17 | 2E-154 | PubMed |
| Thrombomodulin levels | — | OR 0.66 | 9E-59 | PubMed |
| TM levels | — | OR 1.32 | 3E-11 | PubMed |
| THBD protein levels | A | OR 0.46 | 1E-10 | PubMed |
Sources
- dbSNP: rs1042579 — the reference record
- ClinVar — clinical interpretations submitted by laboratories
- SNPedia — community-written summaries
- GWAS Catalog — association studies