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Electrocardiogram morphology (amplitude at temporal datapoints)

IFRD1 · rs3128384

What the study found

Who was studied 63,706 European and unknown ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.035 lower (95% confidence interval 0.024-0.046); p = 1 × 10−9.

How common The C allele had a frequency of about 61% in the people studied.

Where it sits Chromosome 7, band 7q31.1 — in the 5′ untranslated region of LSMEM1.

What each result means

C/C Two copies of the version the research linked to Electrocardiogram morphology (amplitude at temporal datapoints). 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 Electrocardiogram morphology (amplitude at temporal datapoints). That is a smaller link than two copies.
T/T No copy of the version the research linked to Electrocardiogram morphology (amplitude at temporal datapoints). This is the starting point the study compared everyone against.
Source

Questions about rs3128384

What is rs3128384?

rs3128384 is a single position in the genome, in or near the IFRD1 gene. Published research associates it with electrocardiogram morphology (amplitude at temporal datapoints). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs3128384 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 rs3128384 come from?

GWAS Catalog, Cell systems 2020, PMID:32916098. 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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Electrocardiogram morphology (amplitude at temporal datapoints) (rs3128384). MyGeneLog™. https://www.mygenelog.com/variants/rs3128384

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