Standard
Electrocardiographic conduction measures
SCN5A · rs1805126
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 Electrocardiographic conduction measures compared to the general population.
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Electrocardiographic conduction measures.
G/G
Published research associates this genotype with typical/baseline likelihood of Electrocardiographic conduction measures — no copies of the reported risk allele.
Source
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk
Ritchie MD,
Denny JC,
Zuvich RL,
Crawford DC,
Schildcrout JS,
Bastarache L,
Ramirez AH,
Mosley JD,
Pulley JM,
Basford MA,
Bradford Y,
Rasmussen LV
and 15 more — show all
Pathak J,
Chute CG,
Kullo IJ,
McCarty CA,
Chisholm RL,
Kho AN,
Carlson CS,
Larson EB,
Jarvik GP,
Sotoodehnia N,
Manolio TA,
Li R,
Masys DR,
Haines JL,
Roden DM
Circulation · 2013 · PMID 23463857
Questions about rs1805126
What is rs1805126?
rs1805126 is a single position in the genome, in or near the SCN5A gene. Published research associates it with electrocardiographic conduction measures. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1805126 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 rs1805126 come from?
GWAS Catalog, Circulation 2013, PMID:23463857. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants