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Electrocardiogram morphology (amplitude at temporal datapoints)

ATP1B1 · rs1200130

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 0.0551 lower (95% confidence interval 0.042-0.068); p = 2 × 10−16.

How common The C allele had a frequency of about 78% in the people studied.

Where it sits Chromosome 1, band 1q24.2 — in an intron of ATP1B1.

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 rs1200130

What is rs1200130?

rs1200130 is a single position in the genome, in or near the ATP1B1 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 rs1200130 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 rs1200130 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) (rs1200130). MyGeneLog™. https://www.mygenelog.com/variants/rs1200130

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