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Frontal QRS-T angle

near DND1P1 · rs1724411

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 134,567 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0389 lower (95% confidence interval 0.029-0.049); p = 3 × 10⁻¹³.

How common The T allele had a frequency of about 78% in the people studied.

Where it sits Chromosome 17, band 17q21.31 — between genes, 5.6 kb from DND1P1.

What each result means

C/C No copy of the version the research linked to Frontal QRS-T angle. This is the starting point the study compared everyone against.

C/T One copy of the version the research linked to Frontal QRS-T angle. That is a smaller link than two copies.

T/T Two copies of the version the research linked to Frontal QRS-T angle. That is the strongest link of the three results. A link in a study is not a diagnosis.

Source

Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease

Young WJ, Haessler J, Benjamins JW, Repetto L, Yao J, Isaacs A, Harper AR, Ramirez J, Garnier S, van Duijvenboden S, Baldassari AR, Concas MP

and 82 more — show all

Duong T, Foco L, Isaksen JL, Mei H, Noordam R, Nursyifa C, Richmond A, Santolalla ML, Sitlani CM, Soroush N, Thériault S, Trompet S, Aeschbacher S, Ahmadizar F, Alonso A, Brody JA, Campbell A, Correa A, Darbar D, De Luca A, Deleuze JF, Ellervik C, Fuchsberger C, Goel A, Grace C, Guo X, Hansen T, Heckbert SR, Jackson RD, Kors JA, Lima-Costa MF, Linneberg A, Macfarlane PW, Morrison AC, Navarro P, Porteous DJ, Pramstaller PP, Reiner AP, Risch L, Schotten U, Shen X, Sinagra G, Soliman EZ, Stoll M, Tarazona-Santos E, Tinker A, Trajanoska K, Villard E, Warren HR, Whitsel EA, Wiggins KL, Arking DE, Avery CL, Conen D, Girotto G, Grarup N, Hayward C, Jukema JW, Mook-Kanamori DO, Olesen MS, Padmanabhan S, Psaty BM, Pattaro C, Ribeiro ALP, Rotter JI, Stricker BH, van der Harst P, van Duijn CM, Verweij N, Wilson JG, Orini M, Charron P, Watkins H, Kooperberg C, Lin HJ, Wilson JF, Kanters JK, Sotoodehnia N, Mifsud B, Lambiase PD, Tereshchenko LG, Munroe PB

Nature communications · 2023 · PMID 36918541 · open access

Questions about rs1724411

What is rs1724411?

rs1724411 is a single position in the genome, in or near the near DND1P1 gene. Published research associates it with frontal qrs-t angle. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1724411 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 rs1724411 come from?

GWAS Catalog, Nature communications 2023, PMID:36918541. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Frontal QRS-T angle (rs1724411). MyGeneLog™. https://www.mygenelog.com/variants/rs1724411

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