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FEV1

PPP6R2 · rs113111175

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 321,047 European ancestry individuals; replicated in 79,005 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.022 higher (95% confidence interval 0.015-0.029); p = 1 × 10⁻⁹.

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

Where it sits Chromosome 22, band 22q13.33 — in an intron of PPP6R2.

What each result means

C/C No copy of the version the research linked to FEV1. This is the starting point the study compared everyone against.

C/T One copy of the version the research linked to FEV1. That is a smaller link than two copies.

T/T Two copies of the version the research linked to FEV1. That is the strongest link of the three results. A link in a study is not a diagnosis.

Source

New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

Shrine N, Guyatt AL, Erzurumluoglu AM, Jackson VE, Hobbs BD, Melbourne CA, Batini C, Fawcett KA, Song K, Sakornsakolpat P, Li X, Boxall R

and 99 more — show all

Reeve NF, Obeidat M, Zhao JH, Wielscher M, Weiss S, Kentistou KA, Kentistou KA, Cook JP, Sun BB, Zhou J, Hui J, Karrasch S, Imboden M, Harris SE, Marten J, Enroth S, Kerr SM, Surakka I, Vitart V, Lehtimäki T, Allen RJ, Bakke PS, Beaty TH, Bleecker ER, Bossé Y, Brandsma CA, Chen Z, Crapo JD, Danesh J, DeMeo DL, Dudbridge F, Ewert R, Gieger C, Gulsvik A, Hansell AL, Hao K, Hoffman JD, Hokanson JE, Homuth G, Joshi PK, Joubert P, Langenberg C, Li X, Li L, Lin K, Lind L, Locantore N, Luan J, Mahajan A, Maranville JC, Murray A, Nickle DC, Packer R, Parker MM, Paynton ML, Porteous DJ, Porteous DJ, Prokopenko D, Qiao D, Rawal R, Runz H, Sayers I, Sin DD, Smith BH, Soler Artigas M, Sparrow D, Tal-Singer R, Timmers PRHJ, Van den Berge M, Whittaker JC, Woodruff PG, Yerges-Armstrong LM, Troyanskaya OG, Raitakari OT, Kähönen M, Polašek O, Gyllensten U, Rudan I, Deary IJ, Probst-Hensch NM, Schulz H, James AL, Wilson JF, Stubbe B, Zeggini E, Jarvelin MR, Wareham N, Silverman EK, Hayward C, Morris AP, Butterworth AS, Scott RA, Walters RG, Meyers DA, Cho MH, Strachan DP, Hall IP, Tobin MD, Wain LV

Understanding Society Scientific Group

Nature genetics · 2019 · PMID 30804560 · open access

Questions about rs113111175

What is rs113111175?

rs113111175 is a single position in the genome, in or near the PPP6R2 gene. Published research associates it with fev1. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs113111175 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 rs113111175 come from?

GWAS Catalog, Nature genetics 2019, PMID:30804560. 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.

FEV1 (rs113111175). MyGeneLog™. https://www.mygenelog.com/variants/rs113111175

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