Genetic variant
rs913678
rs913678 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 rs913678 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 rs913678, 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
- rs913678
- Position
- chr20:50338887
Genome-wide association studies (20)
| Trait | Risk allele | OR / beta | P-value | Study |
|---|---|---|---|---|
| monocyte (fraction, mean, inv-norm transformed) | T | β 0.099 | 2E-196 | PubMed |
| Monocyte percentage (UKB data field 30190) | C | β 0.049 | 1E-135 | PubMed |
| monocyte (fraction, maximum, inv-norm transformed) | T | β 0.074 | 1E-122 | PubMed |
| monocyte (fraction, mean, inv-norm transformed) | T | β 0.083 | 9E-122 | PubMed |
| Monocyte percentage of white cells | C | β 0.056 | 8E-119 | PubMed |
| Monocyte count (UKB data field 30130) | C | β 0.044 | 1E-111 | PubMed |
| Monocyte count | C | β 0.05 | 3E-97 | PubMed |
| monocyte (fraction, maximum, inv-norm transformed) | T | β 0.067 | 2E-92 | PubMed |
| monocyte (fraction, minimum, inv-norm transformed) | T | β 0.057 | 9E-71 | PubMed |
| Height | T | β 0.011 | 2E-58 | PubMed |
| Monocyte percentage of white cells | C | β 0.055 | 3E-47 | PubMed |
| Lymphocyte-to-monocyte ratio | T | — | 5E-46 | PubMed |
| Granulocyte percentage of myeloid white cells | C | β 0.049 | 2E-37 | PubMed |
| Monocyte count | C | β 0.048 | 2E-36 | PubMed |
| Mouth ulcers | C | OR 1.06 | 3E-36 | PubMed |
| Monocyte count | T | — | 5E-31 | PubMed |
| DMP1 protein levels | C | β 0.048 | 2E-18 | PubMed |
| LILRA5 protein levels | C | β 0.038 | 1E-12 | PubMed |
| monocyte (absolute count, mean, inv-norm transformed) | T | β 0.049 | 3E-12 | PubMed |
| Height | — | β 0.012 | 2E-11 | PubMed |
Sources
- dbSNP: rs913678 — the reference record
- ClinVar — clinical interpretations submitted by laboratories
- SNPedia — community-written summaries
- GWAS Catalog — association studies