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Right bundle branch block (PheCode 426.31)

UGT8 · rs13115816

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 the study found

Who was studied 1,024 African American or Afro-Caribbean cases, 119,414 African American or Afro-Caribbean controls, 7,059 European ancestry cases, 434,478 European ancestry controls, 536 Hispanic or Latin American cases, 58,533 Hispanic or Latin American controls.

The effect Each copy of the A allele shifted the measure 0.276 higher (95% confidence interval 0.19-0.36); p = 4 × 10−16.

How common The A allele had a frequency of about 12% in the people studied.

Where it sits Chromosome 4, band 4q26 — in an intron of UGT8.

What each result means

A/A Two copies of the version the research linked to Right bundle branch block (PheCode 426.31). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Right bundle branch block (PheCode 426.31). That is a smaller link than two copies.
G/G No copy of the version the research linked to Right bundle branch block (PheCode 426.31). This is the starting point the study compared everyone against.
Source
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Verma A, Huffman JE, Rodriguez A, Conery M, Liu M, Ho YL, Kim Y, Heise DA, Guare L, Panickan VA, Garcon H, Linares F
and 59 more — show all
Costa L, Goethert I, Tipton R, Honerlaw J, Davies L, Whitbourne S, Cohen J, Posner DC, Sangar R, Murray M, Wang X, Dochtermann DR, Devineni P, Shi Y, Nandi TN, Assimes TL, Brunette CA, Carroll RJ, Clifford R, Duvall S, Gelernter J, Hung A, Iyengar SK, Joseph J, Kember R, Kranzler H, Kripke CM, Levey D, Luoh SW, Merritt VC, Overstreet C, Deak JD, Grant SFA, Polimanti R, Roussos P, Shakt G, Sun YV, Tsao N, Venkatesh S, Voloudakis G, Justice A, Begoli E, Ramoni R, Tourassi G, Pyarajan S, Tsao P, O'Donnell CJ, Muralidhar S, Moser J, Casas JP, Bick AG, Zhou W, Cai T, Voight BF, Cho K, Gaziano JM, Madduri RK, Damrauer S, Liao KP
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access

Questions about rs13115816

What is rs13115816?

rs13115816 is a single position in the genome, in or near the UGT8 gene. Published research associates it with right bundle branch block (phecode 426.31). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs13115816 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 rs13115816 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Right bundle branch block (PheCode 426.31) (rs13115816). MyGeneLog™. https://www.mygenelog.com/variants/rs13115816

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