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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 622 Han Chinese ancestry cases, 8,853 Han Chinese ancestry controls; replicated in 646 Han Chinese ancestry cases, 8,810 Han Chinese ancestry controls.
The effect
Each copy of the T allele carried 0.37 times the odds of Pulmonary embolism (95% confidence interval 0.28-0.49); p = 1 × 10−12.
How common The T allele had a frequency of about 6% in the people studied.
Where it sits Chromosome 8, band 8p12 — between genes, 15.3 kb from LINC02099.
What each result means
G/GNo copy of the version the research linked to Pulmonary embolism. This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to Pulmonary embolism. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Pulmonary embolism. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs35801946 is a single position in the genome, in or near the near LINC02099 gene. Published research associates it with pulmonary embolism. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs35801946 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 rs35801946 come from?
GWAS Catalog, BMC medicine 2023, PMID:37076872. 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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