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Left ventricular end systole anterolateral wall thickness

ZNF592 · rs35630683

What the study found

Who was studied 41,646 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.07 lower (95% confidence interval 0.05-0.09); p = 3 × 10−20.

Where it sits Chromosome 15, band 15q25.3 — in the 3′ untranslated region of ZNF592.

What each result means

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

Questions about rs35630683

What is rs35630683?

rs35630683 is a single position in the genome, in or near the ZNF592 gene. Published research associates it with left ventricular end systole anterolateral 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 rs35630683 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 rs35630683 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 anterolateral wall thickness (rs35630683). MyGeneLog™. https://www.mygenelog.com/variants/rs35630683

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