Genetic variant
rs1871859
rs1871859 is a single-letter difference in human DNA, on chromosome 6. 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 rs1871859 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 rs1871859, 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
- rs1871859
- Position
- chr6:151577371
Genome-wide association studies (20)
| Trait | Risk allele | OR / beta | P-value | Study |
|---|---|---|---|---|
| Heel bone mineral density | — | OR 0.11 | 5E-255 | PubMed |
| Heel bone mineral density | C | β 0.073 | 2E-101 | PubMed |
| Bone density T-score | — | — | 1E-54 | PubMed |
| Bone density Z-score | — | — | 2E-54 | PubMed |
| Mean bone marrow fat fraction of left and right proximal femur | T | OR 0.12 | 2E-26 | PubMed |
| Total cholesterol levels | — | — | 3E-23 | PubMed |
| Total cholesterol levels | T | β 0.016 | 4E-20 | PubMed |
| Total cholesterol levels | T | β 0.02 | 1E-17 | PubMed |
| Bone stiffness index | — | — | 2E-17 | PubMed |
| Low density lipoprotein cholesterol levels | — | — | 2E-17 | PubMed |
| Low-density lipoprotein levels | T | β 0.015 | 2E-15 | PubMed |
| Low density lipoprotein cholesterol levels | T | β 0.018 | 1E-14 | PubMed |
| Non-HDL cholesterol levels | — | — | 4E-14 | PubMed |
| ESM1 protein levels | T | β 0.063 | 5E-14 | PubMed |
| Phosphate levels (UKB data field 30810) | T | β 0.022 | 6E-13 | PubMed |
| Ultradistal forearm bone mineral density | — | OR 0.11 | 8E-13 | PubMed |
| Bone mineral density | — | — | 9E-13 | PubMed |
| Non-HDL cholesterol levels | T | β 0.02 | 9E-13 | PubMed |
| GFRAL protein levels | T | β 0.056 | 3E-12 | PubMed |
| Lymphocyte count | T | β 0.022 | 2E-11 | PubMed |
Sources
- dbSNP: rs1871859 — the reference record
- ClinVar — clinical interpretations submitted by laboratories
- SNPedia — community-written summaries
- GWAS Catalog — association studies