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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 408,112 British individuals.
The effect
Each copy of the A allele shifted the measure 0.018 lower (95% confidence interval 0.014-0.022); p = 4 × 10−16.
How common The A allele had a frequency of about 47% in the people studied.
Where it sits Chromosome 17, band 17q11.2 — in the 3′ untranslated region of ABHD15-AS1.
What each result means
A/ATwo copies of the version the research linked to Lymphocyte count. 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 Lymphocyte count. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Lymphocyte count. This is the starting point the study compared everyone against.
rs3809789 is a single position in the genome, in or near the SSH2 gene. Published research associates it with lymphocyte count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs3809789 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 rs3809789 come from?
GWAS Catalog, Cell 2020, PMID:32888494. 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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