C/CPublished research associates this genotype with typical/baseline likelihood of Urinary albumin excretion — 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 Urinary albumin excretion.
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Urinary albumin excretion compared to the general population.
American journal of human genetics · 2018 · PMID 30220432
Questions about rs112607182
What is rs112607182?
rs112607182 is a single position in the genome, in or near the PRKCI gene. Published research associates it with urinary albumin excretion. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs112607182 linked to?
On MyGeneLog this position is linked to Kidney Function. The research behind each link, and its sources, are set out on that condition page.
Does having rs112607182 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 rs112607182 come from?
GWAS Catalog, Am J Hum Genet 2018, PMID:30220432. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.