Standard

IgA nephropathy

LYN · rs75413466

Where this position leads

Condition: IgA Nephropathy

rs75413466 Condition: IgA Nephropathy IgA Nephropathy Condition rs75413466 rs75413466 LYN

What the study found

Who was studied 5,556 European ancestry cases, 21,178 European ancestry controls, 4,590 East Asian ancestry cases, 7,573 East Asian ancestry controls.

The effect The reported allele is A; the catalogue records no effect size ; p = 1 × 10−10.

Where it sits Chromosome 8, band 8q12.1 — in an intron of LYN.

What each result means

A/A Two copies of the version the research linked to IgA nephropathy. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to IgA nephropathy. That is a smaller link than two copies.
G/G No copy of the version the research linked to IgA nephropathy. This is the starting point the study compared everyone against.
Source

Questions about rs75413466

What is rs75413466?

rs75413466 is a single position in the genome, in or near the LYN gene. Published research associates it with iga 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 rs75413466 linked to?

On MyGeneLog this position is linked to IgA Nephropathy. The research behind each link, and its sources, are set out on that condition page.

Does having rs75413466 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 rs75413466 come from?

GWAS Catalog, Nature genetics 2023, PMID:37337107. 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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IgA nephropathy (rs75413466). MyGeneLog™. https://www.mygenelog.com/variants/rs75413466

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