C/CPublished research associates this genotype with typical/baseline likelihood of Nodular sclerosis Hodgkin lymphoma — no copies of the reported risk allele.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Nodular sclerosis Hodgkin lymphoma.
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Nodular sclerosis Hodgkin lymphoma compared to the general population.
Nature communications · 2017 · PMID 29196614 · open access
Questions about rs3781093
What is rs3781093?
rs3781093 is a single position in the genome, in or near the GATA3 gene. Published research associates it with nodular sclerosis hodgkin lymphoma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs3781093 linked to?
On MyGeneLog this position is linked to Nodular Sclerosis Hodgkin Lymphoma. The research behind each link, and its sources, are set out on that condition page.
Does having rs3781093 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 rs3781093 come from?
GWAS Catalog, Nat Commun 2017, PMID:29196614. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.