NFATC3 c.1402-2432G>A

Variant ID: 16-68189340-G-A

NM_173165.2(NFATC3):c.1402-2432G>A

This variant was identified in 12 publications

View GRCh38 version.




Publications:


Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.

Nature Communications
Lagou, Vasiliki V; Mägi, Reedik R; Hottenga, Jouke- Jan JJ; Grallert, Harald H; Perry, John R B JRB; Bouatia-Naji, Nabila N; Marullo, Letizia L; Rybin, Denis D; Jansen, Rick R; Min, Josine L JL; Dimas, Antigone S AS; Ulrich, Anna A; Zudina, Liudmila L; Gådin, Jesper R JR; Jiang, Longda L; Faggian, Alessia A; Bonnefond, Amélie A; Fadista, Joao J; Stathopoulou, Maria G MG; Isaacs, Aaron A; Willems, Sara M SM; Navarro, Pau P; Tanaka, Toshiko T; Jackson, Anne U AU; Montasser, May E ME; O'Connell, Jeff R JR; Bielak, Lawrence F LF; Webster, Rebecca J RJ; Saxena, Richa R; Stafford, Jeanette M JM; Pourcain, Beate St BS; Timpson, Nicholas J NJ; Salo, Perttu P; Shin, So-Youn SY; Amin, Najaf N; Smith, Albert V AV; Li, Guo G; Verweij, Niek N; Goel, Anuj A; Ford, Ian I; Johnson, Paul C D PCD; Johnson, Toby T; Kapur, Karen K; Thorleifsson, Gudmar G; Strawbridge, Rona J RJ; Rasmussen-Torvik, Laura J LJ; Esko, Tõnu T; Mihailov, Evelin E; Fall, Tove T; Fraser, Ross M RM; Mahajan, Anubha A; Kanoni, Stavroula S; Giedraitis, Vilmantas V; Kleber, Marcus E ME; Silbernagel, Günther G; Meyer, Julia J; Müller-Nurasyid, Martina M; Ganna, Andrea A; Sarin, Antti-Pekka AP; Yengo, Loic L; Shungin, Dmitry D; Luan, Jian'an J; Horikoshi, Momoko M; An, Ping P; Sanna, Serena S; Boettcher, Yvonne Y; Rayner, N William NW; Nolte, Ilja M IM; Zemunik, Tatijana T; Iperen, Erik van EV; Kovacs, Peter P; Hastie, Nicholas D ND; Wild, Sarah H SH; McLachlan, Stela S; Campbell, Susan S; Polasek, Ozren O; Carlson, Olga O; Egan, Josephine J; Kiess, Wieland W; Willemsen, Gonneke G; Kuusisto, Johanna J; Laakso, Markku M; Dimitriou, Maria M; Hicks, Andrew A AA; Rauramaa, Rainer R; Bandinelli, Stefania S; Thorand, Barbara B; Liu, Yongmei Y; Miljkovic, Iva I; Lind, Lars L; Doney, Alex A; Perola, Markus M; Hingorani, Aroon A; Kivimaki, Mika M; Kumari, Meena M; Bennett, Amanda J AJ; Groves, Christopher J CJ; Herder, Christian C; Koistinen, Heikki A HA; Kinnunen, Leena L; Faire, Ulf de U; Bakker, Stephan J L SJL; Uusitupa, Matti M; Palmer, Colin N A CNA; Jukema, J Wouter JW; Sattar, Naveed N; Pouta, Anneli A; Snieder, Harold H; Boerwinkle, Eric E; Pankow, James S JS; Magnusson, Patrik K PK; Krus, Ulrika U; Scapoli, Chiara C; de Geus, Eco J C N EJCN; Blüher, Matthias M; Wolffenbuttel, Bruce H R BHR; Province, Michael A MA; Abecasis, Goncalo R GR; Meigs, James B JB; Hovingh, G Kees GK; Lindström, Jaana J; Wilson, James F JF; Wright, Alan F AF; Dedoussis, George V GV; Bornstein, Stefan R SR; Schwarz, Peter E H PEH; Tönjes, Anke A; Winkelmann, Bernhard R BR; Boehm, Bernhard O BO; März, Winfried W; Metspalu, Andres A; Price, Jackie F JF; Deloukas, Panos P; Körner, Antje A; Lakka, Timo A TA; Keinanen-Kiukaanniemi, Sirkka M SM; Saaristo, Timo E TE; Bergman, Richard N RN; Tuomilehto, Jaakko J; Wareham, Nicholas J NJ; Langenberg, Claudia C; Männistö, Satu S; Franks, Paul W PW; Hayward, Caroline C; Vitart, Veronique V; Kaprio, Jaakko J; Visvikis-Siest, Sophie S; Balkau, Beverley B; Altshuler, David D; Rudan, Igor I; Stumvoll, Michael M; Campbell, Harry H; van Duijn, Cornelia M CM; Gieger, Christian C; Illig, Thomas T; Ferrucci, Luigi L; Pedersen, Nancy L NL; Pramstaller, Peter P PP; Boehnke, Michael M; Frayling, Timothy M TM; Shuldiner, Alan R AR; Peyser, Patricia A PA; Kardia, Sharon L R SLR; Palmer, Lyle J LJ; Penninx, Brenda W BW; Meneton, Pierre P; Harris, Tamara B TB; Navis, Gerjan G; Harst, Pim van der PV; Smith, George Davey GD; Forouhi, Nita G NG; Loos, Ruth J F RJF; Salomaa, Veikko V; Soranzo, Nicole N; Boomsma, Dorret I DI; Groop, Leif L; Tuomi, Tiinamaija T; Hofman, Albert A; Munroe, Patricia B PB; Gudnason, Vilmundur V; Siscovick, David S DS; Watkins, Hugh H; Lecoeur, Cecile C; Vollenweider, Peter P; Franco-Cereceda, Anders A; Eriksson, Per P; Jarvelin, Marjo-Riitta MR; Stefansson, Kari K; Hamsten, Anders A; Nicholson, George G; Karpe, Fredrik F; Dermitzakis, Emmanouil T ET; Lindgren, Cecilia M CM; McCarthy, Mark I MI; Froguel, Philippe P; Kaakinen, Marika A MA; Lyssenko, Valeriya V; Watanabe, Richard M RM; Ingelsson, Erik E; Florez, Jose C JC; Dupuis, Josée J; Barroso, Inês I; Morris, Andrew P AP; Prokopenko, Inga I; ,
Publication Date: 2021-01-05

Variant appearance in text: rs8044995
PubMed Link: 33402679
Variant Present in the following documents:
  • Main text
  • 41467_2020_Article_19366.pdf
View BVdb publication page



Correlated expression analysis of genes implicated in schizophrenia: identification of putative disease-related pathways.

New Horizons In Translational Medicine
Liedtke, Erin I EI; Zhang, Sirey S; Thompson, John A JA; Sillau, Stefan S; Gault, Judith J
Publication Date: 2017-01

Variant appearance in text: rs8044995
PubMed Link: 32864408
Variant Present in the following documents:
  • Main text
View BVdb publication page



CalPen (Calculator of Penetrance), a web-based tool to estimate penetrance in complex genetic disorders.

Plos One
Addepalli, Aditya A; Kalyani, Sakhare S; Singh, Minali M; Bandyopadhyay, Debashree D; Mohan, K Naga KN
Publication Date: 2020

Variant appearance in text: rs8044995
PubMed Link: 31995602
Variant Present in the following documents:
  • Main text
  • pone.0228156.pdf
View BVdb publication page



Comparison of quantitative trait loci methods: Total expression and allelic imbalance method in brain RNA-seq.

Plos One
Gådin, Jesper R JR; Buil, Alfonso A; Colantuoni, Carlo C; Jaffe, Andrew E AE; Nielsen, Jacob J; Shin, Joo-Heon JH; Hyde, Thomas M TM; Kleinman, Joel E JE; , ; Plath, Niels N; Eriksson, Per P; Brunak, Søren S; Didriksen, Michael M; Weinberger, Daniel R DR; Folkersen, Lasse L
Publication Date: 2019

Variant appearance in text: rs8044995
PubMed Link: 31206532
Variant Present in the following documents:
  • Main text
View BVdb publication page



A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data.

Nature Neuroscience
Wang, Quan Q; Chen, Rui R; Cheng, Feixiong F; Wei, Qiang Q; Ji, Ying Y; Yang, Hai H; Zhong, Xue X; Tao, Ran R; Wen, Zhexing Z; Sutcliffe, James S JS; Liu, Chunyu C; Cook, Edwin H EH; Cox, Nancy J NJ; Li, Bingshan B
Publication Date: 2019-05

Variant appearance in text: rs8044995
PubMed Link: 30988527
Variant Present in the following documents:
  • NIHMS1523940-supplement-3.pdf
View BVdb publication page



Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates.

Nature Communications
Dashti, Hassan S HS; Jones, Samuel E SE; Wood, Andrew R AR; Lane, Jacqueline M JM; van Hees, Vincent T VT; Wang, Heming H; Rhodes, Jessica A JA; Song, Yanwei Y; Patel, Krunal K; Anderson, Simon G SG; Beaumont, Robin N RN; Bechtold, David A DA; Bowden, Jack J; Cade, Brian E BE; Garaulet, Marta M; Kyle, Simon D SD; Little, Max A MA; Loudon, Andrew S AS; Luik, Annemarie I AI; Scheer, Frank A J L FAJL; Spiegelhalder, Kai K; Tyrrell, Jessica J; Gottlieb, Daniel J DJ; Tiemeier, Henning H; Ray, David W DW; Purcell, Shaun M SM; Frayling, Timothy M TM; Redline, Susan S; Lawlor, Deborah A DA; Rutter, Martin K MK; Weedon, Michael N MN; Saxena, Richa R
Publication Date: 2019-03-07

Variant appearance in text: rs8044995
PubMed Link: 30846698
Variant Present in the following documents:
  • 41467_2019_Article_8917.pdf
View BVdb publication page



Immediate Early Genes Anchor a Biological Pathway of Proteins Required for Memory Formation, Long-Term Depression and Risk for Schizophrenia.

Frontiers In Behavioral Neuroscience
Marballi, Ketan K KK; Gallitano, Amelia L AL
Publication Date: 2018

Variant appearance in text: rs8044995
PubMed Link: 29520222
Variant Present in the following documents:
  • Table_1.xlsx, sheet 1
View BVdb publication page



Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.

Plos One
Forstner, Andreas J AJ; Hecker, Julian J; Hofmann, Andrea A; Maaser, Anna A; Reinbold, Céline S CS; Mühleisen, Thomas W TW; Leber, Markus M; Strohmaier, Jana J; Degenhardt, Franziska F; Treutlein, Jens J; Mattheisen, Manuel M; Schumacher, Johannes J; Streit, Fabian F; Meier, Sandra S; Herms, Stefan S; Hoffmann, Per P; Lacour, André A; Witt, Stephanie H SH; Reif, Andreas A; Müller-Myhsok, Bertram B; Lucae, Susanne S; Maier, Wolfgang W; Schwarz, Markus M; Vedder, Helmut H; Kammerer-Ciernioch, Jutta J; Pfennig, Andrea A; Bauer, Michael M; Hautzinger, Martin M; Moebus, Susanne S; Schenk, Lorena M LM; Fischer, Sascha B SB; Sivalingam, Sugirthan S; Czerski, Piotr M PM; Hauser, Joanna J; Lissowska, Jolanta J; Szeszenia-Dabrowska, Neonila N; Brennan, Paul P; McKay, James D JD; Wright, Adam A; Mitchell, Philip B PB; Fullerton, Janice M JM; Schofield, Peter R PR; Montgomery, Grant W GW; Medland, Sarah E SE; Gordon, Scott D SD; Martin, Nicholas G NG; Krasnov, Valery V; Chuchalin, Alexander A; Babadjanova, Gulja G; Pantelejeva, Galina G; Abramova, Lilia I LI; Tiganov, Alexander S AS; Polonikov, Alexey A; Khusnutdinova, Elza E; Alda, Martin M; Cruceanu, Cristiana C; Rouleau, Guy A GA; Turecki, Gustavo G; Laprise, Catherine C; Rivas, Fabio F; Mayoral, Fermin F; Kogevinas, Manolis M; Grigoroiu-Serbanescu, Maria M; Becker, Tim T; Schulze, Thomas G TG; Rietschel, Marcella M; Cichon, Sven S; Fier, Heide H; Nöthen, Markus M MM
Publication Date: 2017

Variant appearance in text: rs8044995
PubMed Link: 28166306
Variant Present in the following documents:
  • Main text
View BVdb publication page



OTTO: a new strategy to extract mental disease-relevant combinations of GWAS hits from individuals.

Molecular Psychiatry
Ehrenreich, H H; Mitjans, M M; Van der Auwera, S S; Centeno, T P TP; Begemann, M M; Grabe, H J HJ; Bonn, S S; Nave, K-A KA
Publication Date: 2018-02

Variant appearance in text: rs8044995
PubMed Link: 27922606
Variant Present in the following documents:
  • Main text
  • mp2016208a.pdf
View BVdb publication page



Genome-Wide Association Studies Suggest Limited Immune Gene Enrichment in Schizophrenia Compared to 5 Autoimmune Diseases.

Schizophrenia Bulletin
Pouget, Jennie G JG; Gonçalves, Vanessa F VF; , ; Spain, Sarah L SL; Finucane, Hilary K HK; Raychaudhuri, Soumya S; Kennedy, James L JL; Knight, Jo J
Publication Date: 2016-09

Variant appearance in text: rs8044995
PubMed Link: 27242348
Variant Present in the following documents:
  • Main text
  • sbw059.pdf
View BVdb publication page



Whole-genome sequencing in multiplex families with psychoses reveals mutations in the SHANK2 and SMARCA1 genes segregating with illness.

Molecular Psychiatry
Homann, O R OR; Misura, K K; Lamas, E E; Sandrock, R W RW; Nelson, P P; McDonough, S I SI; DeLisi, L E LE
Publication Date: 2016-12

Variant appearance in text: rs8044995
PubMed Link: 27001614
Variant Present in the following documents:
  • NIHMS753666-supplement-2.xlsx, sheet 2
  • NIHMS753666-supplement-2.xlsx, sheet 11
  • NIHMS753666-supplement-2.xlsx, sheet 10
  • NIHMS753666-supplement-2.xlsx, sheet 9
  • NIHMS753666-supplement-2.xlsx, sheet 7
  • NIHMS753666-supplement-2.xlsx, sheet 6
View BVdb publication page



DISTMIX: direct imputation of summary statistics for unmeasured SNPs from mixed ethnicity cohorts.

Bioinformatics (Oxford, England)
Lee, Donghyung D; Bigdeli, T Bernard TB; Williamson, Vernell S VS; Vladimirov, Vladimir I VI; Riley, Brien P BP; Fanous, Ayman H AH; Bacanu, Silviu-Alin SA
Publication Date: 2015-10-01

Variant appearance in text: rs8044995
PubMed Link: 26059716
Variant Present in the following documents:
  • supp_btv348_distmix_supplementary_data.pdf
View BVdb publication page