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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 43,722 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.181 higher (95% confidence interval 0.12-0.24); p = 7 × 10−9.
How common The C allele had a frequency of about 98% in the people studied.
Where it sits Chromosome 21, band 21q21.1 — between genes, 1.6 kb from RNU6-113P.
What each result means
C/CTwo copies of the version the research linked to Predicted heart recovery rate. 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 Predicted heart recovery rate. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Predicted heart recovery rate. This is the starting point the study compared everyone against.
Cardiovascular digital health journal · 2022 · PMID 36046430 · open access
Questions about rs2846867
What is rs2846867?
rs2846867 is a single position in the genome, in or near the near RNU6-113P gene. Published research associates it with predicted heart recovery rate. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2846867 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 rs2846867 come from?
GWAS Catalog, Cardiovascular digital health journal 2022, PMID:36046430. 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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