FOXO3 c.621+33541T>C

Variant ID: 6-108916573-T-C

NM_001455.3(FOXO3):c.621+33541T>C

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Interactions among IGF-1, AKT2, FOXO1, and FOXO3 variations and between genes and physical activities on physical performance in community-dwelling elders.

Plos One
Li, Tsai-Chung TC; Wu, Ching-Wei CW; Li, Chia-Ing CI; Wu, Fang-Yang FY; Liao, Li-Na LN; Liu, Chiu-Shong CS; Lin, Chih-Hsueh CH; Wang, Mu-Cyun MC; Yang, Chuan-Wei CW; Lin, Cheng-Chieh CC
Publication Date: 2020

Variant appearance in text: rs9480865
PubMed Link: 32986769
Variant Present in the following documents:
  • Main text
  • pone.0239530.pdf
View BVdb publication page



Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits.

Aging Cell
Teumer, Alexander A; Qi, Qibin Q; Nethander, Maria M; Aschard, Hugues H; Bandinelli, Stefania S; Beekman, Marian M; Berndt, Sonja I SI; Bidlingmaier, Martin M; Broer, Linda L; , ; Cappola, Anne A; Ceda, Gian Paolo GP; Chanock, Stephen S; Chen, Ming-Huei MH; Chen, Tai C TC; Chen, Yii-Der Ida YD; Chung, Jonathan J; Del Greco Miglianico, Fabiola F; Eriksson, Joel J; Ferrucci, Luigi L; Friedrich, Nele N; Gnewuch, Carsten C; Goodarzi, Mark O MO; Grarup, Niels N; Guo, Tingwei T; Hammer, Elke E; Hayes, Richard B RB; Hicks, Andrew A AA; Hofman, Albert A; Houwing-Duistermaat, Jeanine J JJ; Hu, Frank F; Hunter, David J DJ; Husemoen, Lise L LL; Isaacs, Aaron A; Jacobs, Kevin B KB; Janssen, Joop A M J L JA; Jansson, John-Olov JO; Jehmlich, Nico N; Johnson, Simon S; Juul, Anders A; Karlsson, Magnus M; Kilpelainen, Tuomas O TO; Kovacs, Peter P; Kraft, Peter P; Li, Chao C; Linneberg, Allan A; Liu, Yongmei Y; Loos, Ruth J F RJ; , ; Lorentzon, Mattias M; Lu, Yingchang Y; Maggio, Marcello M; Magi, Reedik R; Meigs, James J; Mellström, Dan D; Nauck, Matthias M; Newman, Anne B AB; Pollak, Michael N MN; Pramstaller, Peter P PP; Prokopenko, Inga I; Psaty, Bruce M BM; Reincke, Martin M; Rimm, Eric B EB; Rotter, Jerome I JI; Saint Pierre, Aude A; Schurmann, Claudia C; Seshadri, Sudha S; Sjögren, Klara K; Slagboom, P Eline PE; Strickler, Howard D HD; Stumvoll, Michael M; Suh, Yousin Y; Sun, Qi Q; Zhang, Cuilin C; Svensson, Johan J; Tanaka, Toshiko T; Tare, Archana A; Tönjes, Anke A; Uh, Hae-Won HW; van Duijn, Cornelia M CM; van Heemst, Diana D; Vandenput, Liesbeth L; Vasan, Ramachandran S RS; Völker, Uwe U; Willems, Sara M SM; Ohlsson, Claes C; Wallaschofski, Henri H; Kaplan, Robert C RC
Publication Date: 2016-10

Variant appearance in text: rs9480865
PubMed Link: 27329260
Variant Present in the following documents:
  • ACEL-15-811-s001.pdf
View BVdb publication page



Re-annotation of presumed noncoding disease/trait-associated genetic variants by integrative analyses.

Scientific Reports
Chen, Geng G; Yu, Dianke D; Chen, Jiwei J; Cao, Ruifang R; Yang, Juan J; Wang, Huan H; Ji, Xiangjun X; Ning, Baitang B; Shi, Tieliu T
Publication Date: 2015-03-30

Variant appearance in text: rs9480865
PubMed Link: 25819875
Variant Present in the following documents:
  • srep09453-s1.pdf
View BVdb publication page



Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.

Human Molecular Genetics
Baranzini, Sergio E SE; Wang, Joanne J; Gibson, Rachel A RA; Galwey, Nicholas N; Naegelin, Yvonne Y; Barkhof, Frederik F; Radue, Ernst-Wilhelm EW; Lindberg, Raija L P RL; Uitdehaag, Bernard M G BM; Johnson, Michael R MR; Angelakopoulou, Aspasia A; Hall, Leslie L; Richardson, Jill C JC; Prinjha, Rab K RK; Gass, Achim A; Geurts, Jeroen J G JJ; Kragt, Jolijn J; Sombekke, Madeleine M; Vrenken, Hugo H; Qualley, Pamela P; Lincoln, Robin R RR; Gomez, Refujia R; Caillier, Stacy J SJ; George, Michaela F MF; Mousavi, Hourieh H; Guerrero, Rosa R; Okuda, Darin T DT; Cree, Bruce A C BA; Green, Ari J AJ; Waubant, Emmanuelle E; Goodin, Douglas S DS; Pelletier, Daniel D; Matthews, Paul M PM; Hauser, Stephen L SL; Kappos, Ludwig L; Polman, Chris H CH; Oksenberg, Jorge R JR
Publication Date: 2009-02-15

Variant appearance in text: rs9480865
PubMed Link: 19010793
Variant Present in the following documents:
  • Main text
View BVdb publication page