C/CPublished research associates this genotype with typical/baseline likelihood of Subclinical trait of interstitial lung disease (basilar peel-core ratio of high attentuation areas on CT scan) — no copies of the reported risk allele.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Subclinical trait of interstitial lung disease (basilar peel-core ratio of high attentuation areas on CT scan).
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Subclinical trait of interstitial lung disease (basilar peel-core ratio of high attentuation areas on CT scan) compared to the general population.
Respiratory research · 2017 · PMID 28521775 · open access
Questions about rs7852363
What is rs7852363?
rs7852363 is a single position in the genome, in or near the FLJ35282 gene. Published research associates it with subclinical trait of interstitial lung disease (basilar peel-core ratio of high attentuation areas on ct scan). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7852363 linked to?
On MyGeneLog this position is linked to Interstitial Lung Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs7852363 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 rs7852363 come from?
GWAS Catalog, Respir Res 2017, PMID:28521775. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.