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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 39,640 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0591 SD units lower (95% confidence interval 0.045-0.074); p = 1 × 10−15.
How common The T allele had a frequency of about 64% in the people studied.
Where it sits Chromosome 9, band 9q34.3 — between genes, 0.3 kb from NPDC1.
What each result means
C/CNo copy of the version the research linked to Lymphocyte side fluorescence. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Lymphocyte side fluorescence. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Lymphocyte side fluorescence. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2023 · PMID 37596262 · open access
Questions about rs10781534
What is rs10781534?
rs10781534 is a single position in the genome, in or near the near NPDC1 gene. Published research associates it with lymphocyte side fluorescence. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10781534 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 rs10781534 come from?
GWAS Catalog, Nature communications 2023, PMID:37596262. 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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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Lymphocyte side fluorescence (rs10781534). MyGeneLog™. https://www.mygenelog.com/variants/rs10781534