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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 38,000 South Asian ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.049 higher (95% confidence interval 0.035-0.063); p = 2 × 10−11.
Where it sits Chromosome 12, band 12q24.13 — in an intron of HECTD4.
What each result means
C/CTwo copies of the version the research linked to Platelet count. 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 Platelet count. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Platelet count. This is the starting point the study compared everyone against.
Nature communications · 2024 · PMID 39414775 · open access
Questions about rs1468253
What is rs1468253?
rs1468253 is a single position in the genome, in or near the HECTD4 gene. Published research associates it with platelet count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1468253 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 rs1468253 come from?
GWAS Catalog, Nature communications 2024, PMID:39414775. 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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