C/CPublished research associates this genotype with typical/baseline likelihood of Alcohol use disorder (total score) — 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 Alcohol use disorder (total score).
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Alcohol use disorder (total score) compared to the general population.
The American journal of psychiatry · 2019 · PMID 30336701
Questions about rs35040843
What is rs35040843?
rs35040843 is a single position in the genome, in or near the RP11-700E23.3 gene. Published research associates it with alcohol use disorder (total score). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs35040843 linked to?
On MyGeneLog this position is linked to Alcohol Use Disorder. The research behind each link, and its sources, are set out on that condition page.
Does having rs35040843 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 rs35040843 come from?
GWAS Catalog, Am J Psychiatry 2018, PMID:30336701. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.