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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 2,643 Korean ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.6 lower (95% confidence interval 0.42-0.78); p = 5 × 10−11.
How common The A allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 8, band 8q24.3 — a missense change in SHARPIN.
What each result means
A/ATwo copies of the version the research linked to Hippocampal volume. 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 Hippocampal volume. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Hippocampal volume. This is the starting point the study compared everyone against.
Translational psychiatry · 2021 · PMID 34785643 · open access
Questions about rs77359862
What is rs77359862?
rs77359862 is a single position in the genome, in or near the SHARPIN gene. Published research associates it with hippocampal volume. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs77359862 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 rs77359862 come from?
GWAS Catalog, Translational psychiatry 2021, PMID:34785643. 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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