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Who was studied 556 European ancestry cases, 2,338 European ancestry controls.
The effect
Each copy of the T allele carried 2.62 times the odds of Idiopathic membranous nephropathy; p = 1 × 10−42.
How common The T allele had a frequency of about 19% in the people studied.
Where it sits Chromosome 6, band 6p21.33 — in an intron of PSORS1C1.
What each result means
C/CNo copy of the version the research linked to Idiopathic membranous nephropathy. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Idiopathic membranous nephropathy. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Idiopathic membranous nephropathy. That is the strongest link of the three results. A link in a study is not a diagnosis.
The New England journal of medicine · 2011 · PMID 21323541
Questions about rs3130564
What is rs3130564?
rs3130564 is a single position in the genome, in or near the PSORS1C1 gene. Published research associates it with idiopathic membranous nephropathy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs3130564 linked to?
On MyGeneLog this position is linked to Idiopathic Membranous Nephropathy. The research behind each link, and its sources, are set out on that condition page.
Does having rs3130564 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 rs3130564 come from?
GWAS Catalog, The New England journal of medicine 2011, PMID:21323541. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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