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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 1,181 European ancestry cases, 280 African American cases, 54 Hispanic cases, 184 cases, 7,255 European ancestry controls, 2,184 African American controls, 385 Hispanic controls, 450 controls.
The effect
Each copy of the C allele carried 1.31 times the odds of Interstitial lung abnormalities (95% confidence interval 1.19-1.44); p = 3 × 10−9.
How common The C allele had a frequency of about 33% in the people studied.
Where it sits Chromosome 6, band 6q14.3 — between genes, 22.9 kb from HTR1E.
What each result means
A/ANo copy of the version the research linked to Interstitial lung abnormalities. This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Interstitial lung abnormalities. That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Interstitial lung abnormalities. That is the strongest link of the three results. A link in a study is not a diagnosis.
American journal of respiratory and critical care medicine · 2019 · PMID 31339356
Questions about rs7739124
What is rs7739124?
rs7739124 is a single position in the genome, in or near the HTR1E gene. Published research associates it with interstitial lung abnormalities. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7739124 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 rs7739124 come from?
GWAS Catalog, American journal of respiratory and critical care medicine 2019, PMID:31339356. 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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