Genetic variant
rs8756
rs8756 is a single-letter difference in human DNA, on chromosome 12. 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 rs8756 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 rs8756, 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
- rs8756
- Position
- chr12:65965972
Genome-wide association studies (20)
| Trait | Risk allele | OR / beta | P-value | Study |
|---|---|---|---|---|
| Height | C | β 0.057 | 1E-300 | PubMed |
| Height | C | β 0.059 | 1E-300 | PubMed |
| Weight (mean, inv-normal transformed) | C | β 0.073 | 1E-149 | PubMed |
| Weight (minimum, inv-normal transformed) | C | β 0.069 | 3E-143 | PubMed |
| Height | A | β 0.036 | 2E-141 | PubMed |
| Height | C | β 0.055 | 1E-140 | PubMed |
| Weight (maximum, inv-normal transformed) | C | β 0.068 | 5E-128 | PubMed |
| height (mean, inv-normal transformed) | C | β 0.078 | 5E-121 | PubMed |
| Height (maximum, inv-normal transformed) | C | β 0.076 | 3E-119 | PubMed |
| height (minimum, inv-normal transformed) | C | β 0.073 | 3E-116 | PubMed |
| Height | A | β 0.059 | 5E-90 | PubMed |
| What is your height? (cm, inv-normal transformed) | C | β 0.073 | 2E-78 | PubMed |
| FVC | — | — | 1E-63 | PubMed |
| Weight (minimum, inv-normal transformed) | C | β 0.048 | 8E-58 | PubMed |
| FEV1 | — | — | 8E-58 | PubMed |
| Weight (mean, inv-normal transformed) | C | β 0.049 | 1E-55 | PubMed |
| Height | C | β 0.046 | 1E-52 | PubMed |
| Weight (maximum, inv-normal transformed) | C | β 0.047 | 2E-49 | PubMed |
| What is your weight? (pounds, inv-normal transformed) | C | β 0.046 | 2E-39 | PubMed |
| Type 2 diabetes | A | — | 7E-39 | PubMed |
Sources
- dbSNP: rs8756 — the reference record
- ClinVar — clinical interpretations submitted by laboratories
- SNPedia — community-written summaries
- GWAS Catalog — association studies