C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Mean platelet volume compared to the general population.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Mean platelet volume.
T/TPublished research associates this genotype with typical/baseline likelihood of Mean platelet volume — no copies of the reported risk allele.
rs7722711 is a single position in the genome, in or near the IQGAP2 gene. Published research associates it with mean platelet volume. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7722711 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 rs7722711 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 rs7722711 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.