C/CPublished research associates this genotype with typical/baseline likelihood of COVID-19 (critical illness vs population) — 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 COVID-19 (critical illness vs population).
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of COVID-19 (critical illness vs population) compared to the general population.
rs73064425 is a single position in the genome, in or near the LZTFL1 gene. Published research associates it with covid-19 (critical illness vs population). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs73064425 linked to?
On MyGeneLog this position is linked to Abacavir Hypersensitivity (HLA-B*57:01). The research behind each link, and its sources, are set out on that condition page.
Does having rs73064425 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 rs73064425 come from?
GWAS Catalog, Nature 2020, PMID:33307546. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.