Standard
Heart rate
GNG11 · rs180242
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 Heart rate — no copies of the reported risk allele.
A/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Heart rate.
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Heart rate compared to the general population.
Source
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
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Brundel BJ,
Peal DS,
Evans DM,
Nolte IM,
Segrè AV,
Holm H,
Handsaker RE,
Westra HJ,
Johnson T
and 256 more — show all
Isaacs A,
Yang J,
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Zhao JH,
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Nature genetics · 2013 · PMID 23583979
Questions about rs180242
What is rs180242?
rs180242 is a single position in the genome, in or near the GNG11 gene. Published research associates it with heart rate. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs180242 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 rs180242 come from?
GWAS Catalog, Nat Genet 2013, PMID:23583979. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants