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Who was studied 372,047 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 11.1 z score lower; p = 2 × 10−28.
How common The A allele had a frequency of about 22% in the people studied.
Where it sits Chromosome 17, band 17q21.31 — in an intron of MAPT.
What each result means
A/ATwo copies of the version the research linked to Feeling hurt. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Feeling hurt. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Feeling hurt. This is the starting point the study compared everyone against.
Nature communications · 2018 · PMID 29500382 · open access
Questions about rs62061733
What is rs62061733?
rs62061733 is a single position in the genome, in or near the MAPT gene. Published research associates it with feeling hurt. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs62061733 linked to?
On MyGeneLog this position is linked to Irritable Mood. The research behind each link, and its sources, are set out on that condition page.
Does having rs62061733 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 rs62061733 come from?
GWAS Catalog, Nature communications 2018, PMID:29500382. 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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