Standard
P wave duration
CAND2 · rs1467026
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 P wave duration — no copies of the reported risk allele.
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with P wave duration.
G/G
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of P wave duration compared to the general population.
Source
Fifteen Genetic Loci Associated With the Electrocardiographic P Wave
Christophersen IE,
Magnani JW,
Yin X,
Barnard J,
Weng LC,
Arking DE,
Niemeijer MN,
Lubitz SA,
Avery CL,
Duan Q,
Felix SB,
Bis JC
and 40 more — show all
Kerr KF,
Isaacs A,
Müller-Nurasyid M,
Müller C,
North KE,
Reiner AP,
Tinker LF,
Kors JA,
Teumer A,
Petersmann A,
Sinner MF,
Buzkova P,
Smith JD,
Van Wagoner DR,
Völker U,
Waldenberger M,
Peters A,
Meitinger T,
Limacher MC,
Wilhelmsen KC,
Psaty BM,
Hofman A,
Uitterlinden A,
Krijthe BP,
Zhang ZM,
Schnabel RB,
Kääb S,
van Duijn C,
Rotter JI,
Sotoodehnia N,
Dörr M,
Li Y,
Chung MK,
Soliman EZ,
Alonso A,
Whitsel EA,
Stricker BH,
Benjamin EJ,
Heckbert SR,
Ellinor PT
Circulation. Cardiovascular genetics · 2017 · PMID 28794112
Questions about rs1467026
What is rs1467026?
rs1467026 is a single position in the genome, in or near the CAND2 gene. Published research associates it with p wave duration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1467026 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 rs1467026 come from?
GWAS Catalog, Circ Cardiovasc Genet 2017, PMID:28794112. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants