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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 T allele carried 1.68 times the odds of Interstitial lung abnormalities (95% confidence interval 1.39-2.02); p = 5 × 10−9.
How common The T allele had a frequency of about 6% in the people studied.
Where it sits Chromosome 3, band 3q13.12 — in an intron of LINC00882.
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/TOne copy of the version the research linked to Interstitial lung abnormalities. That is a smaller link than two copies.
T/TTwo 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 rs73199442
What is rs73199442?
rs73199442 is a single position in the genome, in or near the FCF1P3 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 rs73199442 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 rs73199442 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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