Genetic variant
rs9298506
rs9298506 is a single-letter difference in human DNA, on chromosome 8. 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 rs9298506 is the catalogue number of one of them. Which letters you carry there — one copy from each parent — is your genotype.
A meta-analysis in 2013 for more than 116,000 individuals showed OR 1.21
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 rs9298506, 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
- rs9298506
- Position
- chr8:54524964
Genome-wide association studies (14)
| Trait | Risk allele | OR / beta | P-value | Study |
|---|---|---|---|---|
| LAYN/ULBP2 protein level ratio | — | OR 0.13 | 7E-54 | PubMed |
| Low density lipoprotein cholesterol levels | — | — | 2E-45 | PubMed |
| Total cholesterol levels | G | β 0.025 | 8E-36 | PubMed |
| Low density lipoprotein cholesterol levels | G | β 0.025 | 2E-35 | PubMed |
| Non-HDL cholesterol levels | G | β 0.028 | 5E-34 | PubMed |
| Height | G | β 0.009 | 4E-29 | PubMed |
| Low density lipoprotein cholesterol levels | — | β 0.031 | 3E-23 | PubMed |
| Direct low density lipoprotein levels (UKB data field 30780) | G | β 0.022 | 3E-18 | PubMed |
| Apolipoprotein B levels | A | β 0.019 | 1E-13 | PubMed |
| LDL cholesterol levels | A | β 0.019 | 3E-13 | PubMed |
| SIGLEC9 protein levels | G | β 0.03 | 3E-13 | PubMed |
| Intracranial aneurysm | A | OR 1.28 | 1E-12 | PubMed |
| Intracranial aneurysm | A | OR 1.35 | 2E-9 | PubMed |
| Coronary artery disease | A | β 0.025 | 3E-8 | PubMed |
Sources
- dbSNP: rs9298506 — the reference record
- ClinVar — clinical interpretations submitted by laboratories
- SNPedia — community-written summaries
- GWAS Catalog — association studies