C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Stem cell growth factor beta levels compared to the general population.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Stem cell growth factor beta levels.
T/TPublished research associates this genotype with typical/baseline likelihood of Stem cell growth factor beta levels — no copies of the reported risk allele.
American journal of human genetics · 2017 · PMID 27989323
Questions about rs116924815
What is rs116924815?
rs116924815 is a single position in the genome, in or near the CLEC11A gene. Published research associates it with stem cell growth factor beta levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs116924815 linked to?
On MyGeneLog this position is linked to MIP-1b (CCL4) Levels. The research behind each link, and its sources, are set out on that condition page.
Does having rs116924815 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs116924815 come from?
GWAS Catalog, Am J Hum Genet 2016, PMID:27989323. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.