Genetic variant
rs4074793
rs4074793 is a single-letter difference in human DNA, on chromosome 5. 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 rs4074793 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 rs4074793, 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
- rs4074793
- Position
- chr5:52897294
Genome-wide association studies (20)
| Trait | Risk allele | OR / beta | P-value | Study |
|---|---|---|---|---|
| Gamma glutamyl transferase levels | A | β 0.069 | 4E-133 | PubMed |
| Gamma glutamyl transferase levels | G | β 0.02 | 2E-95 | PubMed |
| Liver enzyme levels (gamma-glutamyl transferase) | A | β 0.019 | 2E-92 | PubMed |
| Gamma glutamyl transpeptidase | G | β 0.066 | 7E-76 | PubMed |
| CDH2 protein levels | G | β 0.096 | 3E-23 | PubMed |
| Gamma glutamyl transferase levels | — | β 0.073 | 5E-22 | PubMed |
| Alanine aminotransferase levels | A | β 0.026 | 1E-19 | PubMed |
| Heel bone mineral density | — | β 0.033 | 4E-17 | PubMed |
| Heel bone mineral density | — | — | 6E-17 | PubMed |
| Gamma glutamyl transferase levels | — | β 0.065 | 2E-16 | PubMed |
| Heel bone mineral density | A | β 0.028 | 2E-15 | PubMed |
| Alanine aminotransferase levels | G | β 0.006 | 3E-15 | PubMed |
| Liver enzyme levels (alanine transaminase) | A | β 0.006 | 2E-14 | PubMed |
| Lung function (FEV1/FVC) | A | OR 7.48 | 7E-14 | PubMed |
| Alkaline phosphatase (UKB data field 30610) | G | β 0.024 | 3E-13 | PubMed |
| Alanine aminotransferase levels | G | OR 7.3 | 3E-13 | PubMed |
| Alanine aminotransferase levels | G | β 0.025 | 2E-12 | PubMed |
| Gamma glutamyl transferase levels | — | — | 2E-11 | PubMed |
| Serum alkaline phosphatase levels | G | OR 6.56 | 6E-11 | PubMed |
| Liver enzyme levels (gamma-glutamyl transferase) | G | OR 5.5 | 3E-10 | PubMed |
Sources
- dbSNP: rs4074793 — the reference record
- ClinVar — clinical interpretations submitted by laboratories
- SNPedia — community-written summaries
- GWAS Catalog — association studies