Sensitive
Peripheral artery disease
IPO5 · rs9584669
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
C/C
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Peripheral artery disease compared to the general population.
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Peripheral artery disease.
T/T
Published research associates this genotype with typical/baseline likelihood of Peripheral artery disease — no copies of the reported risk allele.
Source
Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population
Matsukura M,
Ozaki K,
Takahashi A,
Onouchi Y,
Morizono T,
Komai H,
Shigematsu H,
Kudo T,
Inoue Y,
Kimura H,
Hosaka A,
Shigematsu K
and 5 more — show all
PloS one · 2015 · PMID 26488411 · open access
Questions about rs9584669
What is rs9584669?
rs9584669 is a single position in the genome, in or near the IPO5 gene. Published research associates it with peripheral artery disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs9584669 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 rs9584669 come from?
GWAS Catalog, PLoS One 2015, PMID:26488411. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants