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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 460,198 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0187 higher (95% confidence interval 0.013-0.025); p = 3 × 10−9.
How common The C allele had a frequency of about 91% in the people studied.
Where it sits Chromosome 13, band 13q14.3 — in an intron of RNASEH2B.
What each result means
C/CTwo copies of the version the research linked to Body shape phenotype PC3. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Body shape phenotype PC3. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Body shape phenotype PC3. This is the starting point the study compared everyone against.
Science advances · 2024 · PMID 38640244 · open access
Questions about rs17650569
What is rs17650569?
rs17650569 is a single position in the genome, in or near the RNASEH2B gene. Published research associates it with body shape phenotype pc3. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs17650569 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 rs17650569 come from?
GWAS Catalog, Science advances 2024, PMID:38640244. 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.
Body shape phenotype PC3 (rs17650569). MyGeneLog™. https://www.mygenelog.com/variants/rs17650569