A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Systolic blood pressure change trajectory compared to the general population.
A/CPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Systolic blood pressure change trajectory.
C/CPublished research associates this genotype with typical/baseline likelihood of Systolic blood pressure change trajectory — no copies of the reported risk allele.
BMC proceedings · 2016 · PMID 27980656 · open access
Questions about rs17112252
What is rs17112252?
rs17112252 is a single position in the genome, in or near the ATOX1 gene. Published research associates it with systolic blood pressure change trajectory. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs17112252 linked to?
On MyGeneLog this position is linked to Blood Pressure. The research behind each link, and its sources, are set out on that condition page.
Does having rs17112252 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 rs17112252 come from?
GWAS Catalog, BMC Proc 2016, PMID:27980656. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.