Standard
Spatial QRS-T angle
near RPL7AP73 · rs9506933
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 96,562 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.034 lower (95% confidence interval 0.024-0.044); p = 3 × 10−10.
How common The A allele had a frequency of about 26% in the people studied.
Where it sits Chromosome 13, band 13q12.12 — between genes, 13.7 kb from RPL7AP73.
What each result means
A/A
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Spatial QRS-T angle compared to the general population.
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Spatial QRS-T angle.
G/G
Published research associates this genotype with typical/baseline likelihood of Spatial QRS-T angle — no copies of the reported risk allele.
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 rs9506933
What is rs9506933?
rs9506933 is a single position in the genome, in or near the near RPL7AP73 gene. Published research associates it with spatial 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 rs9506933 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 rs9506933 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.
Spatial QRS-T angle (rs9506933). MyGeneLog™. https://www.mygenelog.com/variants/rs9506933
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