Sensitive
Resting oxygen saturation in chronic osbtructive pulmonary disease (pulse oxymetry)
LINC00928 · rs8038108
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 each result means
A/A
Published research associates this genotype with typical/baseline likelihood of Resting oxygen saturation in chronic osbtructive pulmonary disease (pulse oxymetry) — no copies of the reported risk allele.
A/C
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Resting oxygen saturation in chronic osbtructive pulmonary disease (pulse oxymetry).
C/C
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Resting oxygen saturation in chronic osbtructive pulmonary disease (pulse oxymetry) compared to the general population.
Source
Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease
McDonald ML,
Cho MH,
Sørheim IC,
Lutz SM,
Castaldi PJ,
Lomas DA,
Coxson HO,
Edwards LD,
MacNee W,
Vestbo J,
Yates JC,
Agusti A
and 19 more — show all
Calverley PM,
Celli B,
Crim C,
Rennard SI,
Wouters EF,
Bakke P,
Tal-Singer R,
Miller BE,
Gulsvik A,
Casaburi R,
Wells JM,
Regan EA,
Make BJ,
Hokanson JE,
Lange C,
Crapo JD,
Beaty TH,
Silverman EK,
Hersh CP
American journal of respiratory cell and molecular biology · 2014 · PMID 24825563
Questions about rs8038108
What is rs8038108?
rs8038108 is a single position in the genome, in or near the LINC00928 gene. Published research associates it with resting oxygen saturation in chronic osbtructive pulmonary disease (pulse oxymetry). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs8038108 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 rs8038108 come from?
GWAS Catalog, Am J Respir Cell Mol Biol 2014, PMID:24825563. 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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