Standard
PR interval
MEIS1 · rs10865355
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 (two copies of the reported risk allele) with a higher likelihood of PR interval compared to the general population.
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with PR interval.
G/G
Published research associates this genotype with typical/baseline likelihood of PR interval — no copies of the reported risk allele.
Source
Genome-wide association studies of the PR interval in African Americans
Smith JG,
Magnani JW,
Palmer C,
Meng YA,
Soliman EZ,
Musani SK,
Kerr KF,
Schnabel RB,
Lubitz SA,
Sotoodehnia N,
Redline S,
Pfeufer A
and 16 more — show all
Müller M,
Evans DS,
Nalls MA,
Liu Y,
Newman AB,
Zonderman AB,
Evans MK,
Deo R,
Ellinor PT,
Paltoo DN,
Newton-Cheh C,
Benjamin EJ,
Mehra R,
Alonso A,
Heckbert SR,
Fox ER
PLoS genetics · 2011 · PMID 21347284 · open access
Questions about rs10865355
What is rs10865355?
rs10865355 is a single position in the genome, in or near the MEIS1 gene. Published research associates it with pr interval. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10865355 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 rs10865355 come from?
GWAS Catalog, PLoS Genet 2011, PMID:21347284. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants