Genetic variant
rs56398830
rs56398830 is a single-letter difference in human DNA, on chromosome 13. 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 rs56398830 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 rs56398830, 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
- rs56398830
- Position
- chr13:103049340
Genome-wide association studies (13)
| Trait | Risk allele | OR / beta | P-value | Study |
|---|---|---|---|---|
| GPA33 protein levels | A | OR 0.75 | 6E-212 | PubMed |
| EPCAM protein levels | A | OR 0.68 | 3E-194 | PubMed |
| SLC51B protein levels | A | OR 0.54 | 3E-101 | PubMed |
| S100A14 protein levels | A | OR 0.49 | 4E-85 | PubMed |
| TSPAN8 protein levels | A | OR 0.37 | 4E-68 | PubMed |
| CXADR protein levels | A | OR 0.36 | 3E-53 | PubMed |
| epithelial cell adhesion molecule levels | — | OR 0.75 | 3E-32 | PubMed |
| S100A16 protein levels | A | OR 0.28 | 1E-22 | PubMed |
| Ep-CAM levels | — | OR 0.8 | 3E-17 | PubMed |
| epithelial cell adhesion molecule levels | A | OR 0.94 | 1E-15 | PubMed |
| Cholelithiasis (UKB data field 20002_1162) | — | OR 1.39 | 6E-14 | PubMed |
| Glycochenodeoxycholate 3-sulfate levels | A | OR 0.49 | 4E-13 | PubMed |
| Gallstone disease | — | OR 1.36 | 2E-12 | PubMed |
Sources
- dbSNP: rs56398830 — the reference record
- ClinVar — clinical interpretations submitted by laboratories
- SNPedia — community-written summaries
- GWAS Catalog — association studies