Genetic variant
rs2306022
rs2306022 is a single-letter difference in human DNA, on chromosome 15. 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 rs2306022 is the catalogue number of one of them. Which letters you carry there — one copy from each parent — is your genotype.
Incorporating epistasis interaction of genetic susceptibility single nucleotide polymorphisms in a lung cancer risk prediction model.
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 rs2306022, 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
- rs2306022
- Position
- chr15:68335825
Genome-wide association studies (17)
| Trait | Risk allele | OR / beta | P-value | Study |
|---|---|---|---|---|
| ITGA11/ITGAV protein level ratio | — | OR 0.5 | 4E-391 | PubMed |
| ITGA11 protein levels | T | OR 0.3 | 1E-230 | PubMed |
| Uterine fibroids | T | β 0.091 | 3E-17 | PubMed |
| Vertex-wise sulcal depth | T | OR 7.65 | 2E-14 | PubMed |
| Whole brain restricted isotropic diffusion (multivariate analysis) | — | — | 1E-13 | PubMed |
| Uterine fibroids | T | OR 0.11 | 4E-13 | PubMed |
| Uterine fibroids | T | OR 0.1 | 4E-11 | PubMed |
| Uterine fibroids | T | β 0.08 | 4E-11 | PubMed |
| Dupuytren's disease | T | OR 1.28 | 9E-11 | PubMed |
| Cortical surface area | T | — | 9E-10 | PubMed |
| Uterine leiomyomata | T | OR 1.09 | 2E-9 | PubMed |
| Dupuytren's disease | — | OR 1.18 | 2E-9 | PubMed |
| Facial morphology (segment 15) | T | — | 6E-9 | PubMed |
| Vertex-wise cortical surface area | T | OR 5.76 | 8E-9 | PubMed |
| Waist-to-hip ratio adjusted for BMI | — | — | 2E-8 | PubMed |
| Facial appearance | — | — | 3E-8 | PubMed |
| Uterine fibroids | T | OR 0.14 | 3E-8 | PubMed |
Sources
- dbSNP: rs2306022 — the reference record
- ClinVar — clinical interpretations submitted by laboratories
- SNPedia — community-written summaries
- GWAS Catalog — association studies