C/CPublished research associates this genotype with typical/baseline likelihood of Systolic blood pressure — no copies of the reported risk allele. (GWAS Catalog, Nature 2011, PMID:21909115)
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Systolic blood pressure. (GWAS Catalog, Nature 2011, PMID:21909115)
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Systolic blood pressure compared to the general population. (GWAS Catalog, Nature 2011, PMID:21909115)
Source: GWAS Catalog, Nature 2011, PMID:21909115
Questions about rs11191548
What is rs11191548?
rs11191548 is a single position in the genome, in or near the NT5C2 gene. Published research associates it with systolic blood pressure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs11191548 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 rs11191548 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 rs11191548 come from?
GWAS Catalog, Nature 2011, PMID:21909115. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.