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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 91,084 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.24 milli-gravities higher; p = 7 × 10−11.
How common The A allele had a frequency of about 65% in the people studied.
Where it sits Chromosome 5, band 5q33.1 — in an intron of LINC01470.
What each result means
A/ATwo copies of the version the research linked to Accelerometer-based physical activity measurement (average acceleration). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/TOne copy of the version the research linked to Accelerometer-based physical activity measurement (average acceleration). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Accelerometer-based physical activity measurement (average acceleration). This is the starting point the study compared everyone against.
International journal of obesity (2005) · 2018 · PMID 29899525 · open access
Questions about rs62398709
What is rs62398709?
rs62398709 is a single position in the genome, in or near the LINC01470 gene. Published research associates it with accelerometer-based physical activity measurement (average acceleration). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs62398709 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 rs62398709 come from?
GWAS Catalog, International journal of obesity (2005) 2018, PMID:29899525. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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