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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 100,453 Chinese Han ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.449 higher (95% confidence interval 0.32-0.58); p = 1 × 10−11.
How common The T allele had a frequency of about 49% in the people studied.
Where it sits Chromosome 16, band 16q24.3 — in an intron of CHMP1A.
What each result means
A/ANo copy of the version the research linked to Pulse pressure (BMI unadjusted). This is the starting point the study compared everyone against.
A/TOne copy of the version the research linked to Pulse pressure (BMI unadjusted). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Pulse pressure (BMI unadjusted). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2024 · PMID 39048560 · open access
Questions about rs75268076
What is rs75268076?
rs75268076 is a single position in the genome, in or near the CHMP1A gene. Published research associates it with pulse pressure (bmi unadjusted). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs75268076 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 rs75268076 come from?
GWAS Catalog, Nature communications 2024, PMID:39048560. 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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