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Left ventricular end systole inferoseptal wall thickness

SPI1 · rs7928419

What the study found

Who was studied 41,984 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.05 lower (95% confidence interval 0.03-0.07); p = 1 × 10−12.

Where it sits Chromosome 11, band 11p11.2 — in an intron of SPI1.

What each result means

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

Questions about rs7928419

What is rs7928419?

rs7928419 is a single position in the genome, in or near the SPI1 gene. Published research associates it with left ventricular end systole inferoseptal wall thickness. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs7928419 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 rs7928419 come from?

GWAS Catalog, Nature communications 2023, PMID:38036550. 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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Left ventricular end systole inferoseptal wall thickness (rs7928419). MyGeneLog™. https://www.mygenelog.com/variants/rs7928419

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