Standard

QRS duration

near CDKN2C · rs11588271

Where this position leads

Condition: Cardiac Conduction Intervals (PR Interval and QRS Duration)

What the study found

Who was studied up to 77,898 European ancestry individuals, up to 7,695 African American individuals; replicated in up to 111,874 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.326 ms lower (95% confidence interval 0.26-0.39); p = 1 × 10⁻²⁰.

How common The A allele had a frequency of about 31% in the people studied.

Where it sits Chromosome 1, band 1p32.3 — between genes, 29.9 kb from CDKN2C.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of QRS duration compared to the general population.

A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with QRS duration.

G/G Published research associates this genotype with typical/baseline likelihood of QRS duration — no copies of the reported risk allele.

Source

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

Prins BP, Mead TJ, Brody JA, Sveinbjornsson G, Ntalla I, Bihlmeyer NA, van den Berg M, Bork-Jensen J, Cappellani S, Van Duijvenboden S, Klena NT, Gabriel GC

and 101 more — show all

Liu X, Gulec C, Grarup N, Haessler J, Hall LM, Iorio A, Isaacs A, Li-Gao R, Lin H, Liu CT, Lyytikäinen LP, Marten J, Mei H, Müller-Nurasyid M, Orini M, Padmanabhan S, Radmanesh F, Ramirez J, Robino A, Schwartz M, van Setten J, Smith AV, Verweij N, Warren HR, Weiss S, Alonso A, Arnar DO, Bots ML, de Boer RA, Dominiczak AF, Eijgelsheim M, Ellinor PT, Guo X, Felix SB, Harris TB, Hayward C, Heckbert SR, Huang PL, Jukema JW, Kähönen M, Kors JA, Lambiase PD, Launer LJ, Li M, Linneberg A, Nelson CP, Pedersen O, Perez M, Peters A, Polasek O, Psaty BM, Raitakari OT, Rice KM, Rotter JI, Sinner MF, Soliman EZ, Spector TD, Strauch K, Thorsteinsdottir U, Tinker A, Trompet S, Uitterlinden A, Vaartjes I, van der Meer P, Völker U, Völzke H, Waldenberger M, Wilson JG, Xie Z, Asselbergs FW, Dörr M, van Duijn CM, Gasparini P, Gudbjartsson DF, Gudnason V, Hansen T, Kääb S, Kanters JK, Kooperberg C, Lehtimäki T, Lin HJ, Lubitz SA, Mook-Kanamori DO, Conti FJ, Newton-Cheh CH, Rosand J, Rudan I, Samani NJ, Sinagra G, Smith BH, Holm H, Stricker BH, Ulivi S, Sotoodehnia N, Apte SS, van der Harst P, Stefansson K, Munroe PB, Arking DE, Lo CW, Jamshidi Y

Genome biology · 2018 · PMID 30012220 · open access

Questions about rs11588271

What is rs11588271?

rs11588271 is a single position in the genome, in or near the near CDKN2C gene. Published research associates it with qrs duration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11588271 linked to?

On MyGeneLog this position is linked to Cardiac Conduction Intervals (PR Interval and QRS Duration). The research behind each link, and its sources, are set out on that condition page.

Does having rs11588271 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 rs11588271 come from?

GWAS Catalog, Genome Biol 2018, PMID:30012220. 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.

QRS duration (rs11588271). MyGeneLog™. https://www.mygenelog.com/variants/rs11588271

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