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Idiopathic membranous nephropathy

c6orf10 · rs3129939

Where this position leads

Condition: Idiopathic Membranous Nephropathy

rs3129939 Condition: Idiopathic Membranous Nephropathy Idiopathic Membranous Nephropathy Condition rs3129939 rs3129939 c6orf10

What the study found

Who was studied 556 European ancestry cases, 2,338 European ancestry controls.

The effect Each copy of the G allele carried 2.60 times the odds of Idiopathic membranous nephropathy; p = 2 × 10−40.

How common The G allele had a frequency of about 18% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — in an intron of TSBP1-AS1.

What each result means

A/A No copy of the version the research linked to Idiopathic membranous nephropathy. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Idiopathic membranous nephropathy. That is a smaller link than two copies.
G/G Two 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.
Source

Questions about rs3129939

What is rs3129939?

rs3129939 is a single position in the genome, in or near the c6orf10 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 rs3129939 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 rs3129939 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 rs3129939 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.

Quoting this page

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Idiopathic membranous nephropathy (rs3129939). MyGeneLog™. https://www.mygenelog.com/variants/rs3129939

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