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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 Up to 27,337 European ancestry individuals, up to 472 Korkulan individuals, up to 1,267 Erasmus Rucphen Family individuals; replicated in Up to 10,617 European ancestry individuals, up to 3,811 African American individuals.
The effect
Each copy of the A allele shifted the measure 0.765 lower (95% confidence interval 0.5-1.04); p = 3 × 10−8.
How common The A allele had a frequency of about 7% in the people studied.
Where it sits Chromosome 5, band 5q11.1 — between genes, 65.7 kb from RNU6-1296P.
What each result means
A/ATwo copies of the version the research linked to Verbal declarative memory. 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 Verbal declarative memory. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Verbal declarative memory. This is the starting point the study compared everyone against.
rs13360092 is a single position in the genome, in or near the ISL1 gene. Published research associates it with verbal declarative memory. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs13360092 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 rs13360092 come from?
GWAS Catalog, Biological psychiatry 2015, PMID:25648963. 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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