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Matrix-remodeling-associated protein 7 levels

SNHG16 · rs2286589

What the study found

Who was studied 3,506 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.308 lower (95% confidence interval 0.26-0.35); p = 3 × 10−41.

How common The A allele had a frequency of about 45% in the people studied.

Where it sits Chromosome 17, band 17q25.1 — in an intron of SNHG16.

What each result means

A/A Two copies of the version the research linked to Matrix-remodeling-associated protein 7 levels. 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 Matrix-remodeling-associated protein 7 levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Matrix-remodeling-associated protein 7 levels. This is the starting point the study compared everyone against.
Source

Questions about rs2286589

What is rs2286589?

rs2286589 is a single position in the genome, in or near the SNHG16 gene. Published research associates it with matrix-remodeling-associated protein 7 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs2286589 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 rs2286589 come from?

GWAS Catalog, Nature genetics 2024, PMID:39528825. 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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Matrix-remodeling-associated protein 7 levels (rs2286589). MyGeneLog™. https://www.mygenelog.com/variants/rs2286589

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