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Left ventricular end systole inferolateral wall thickness

MITF · rs62253183

What the study found

Who was studied 41,947 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.06 higher (95% confidence interval 0.04-0.08); p = 1 × 10−10.

Where it sits Chromosome 3, band 3p13 — in an intron of MITF.

What each result means

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

Questions about rs62253183

What is rs62253183?

rs62253183 is a single position in the genome, in or near the MITF gene. Published research associates it with left ventricular end systole inferolateral 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 rs62253183 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 rs62253183 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 inferolateral wall thickness (rs62253183). MyGeneLog™. https://www.mygenelog.com/variants/rs62253183

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