A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Weight compared to the general population.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Weight.
G/GPublished research associates this genotype with typical/baseline likelihood of Weight — no copies of the reported risk allele.
Nature communications · 2017 · PMID 28548082 · open access
Questions about rs112037309
What is rs112037309?
rs112037309 is a single position in the genome, in or near the INTS12 gene. Published research associates it with weight. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs112037309 linked to?
On MyGeneLog this position is linked to Obesity and Body Weight. The research behind each link, and its sources, are set out on that condition page.
Does having rs112037309 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 rs112037309 come from?
GWAS Catalog, Nat Commun 2017, PMID:28548082. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.