G/GPublished research associates this genotype with typical/baseline likelihood of Sum basophil neutrophil counts — no copies of the reported risk allele.
G/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Sum basophil neutrophil counts.
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Sum basophil neutrophil counts compared to the general population.
rs201950044 is a single position in the genome, in or near the FCGR2B gene. Published research associates it with sum basophil neutrophil counts. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs201950044 linked to?
On MyGeneLog this position is linked to Blood Cell Counts. The research behind each link, and its sources, are set out on that condition page.
Does having rs201950044 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 rs201950044 come from?
GWAS Catalog, Cell 2016, PMID:27863252. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.