NFKB1 c.-8+11308T>C

Variant ID: 4-103434253-T-C

NM_003998.4(NFKB1):c.-8+11308T>C

This variant was identified in 25 publications

View GRCh38 version.




Publications:


Genetic advances in Meniere Disease.

Molecular Biology Reports
Dai, Qingqing Q; Long, Lili L; Zhao, Hui H; Wang, Ruikai R; Zheng, Hong H; Duan, Maoli M
Publication Date: 2022-12-24

Variant appearance in text: rs3774937
PubMed Link: 36565421
Variant Present in the following documents:
  • Main text
  • 11033_2022_Article_8149.pdf
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Genetic Polymorphisms of Nuclear Factor-κB Family Affect the Bone Mineral Density Response to Zoledronic Acid Therapy in Postmenopausal Chinese Women.

Genes
Wang, Wen-Jie WJ; He, Jin-Wei JW; Fu, Wen-Zhen WZ; Wang, Chun C; Zhang, Zhen-Lin ZL
Publication Date: 2022-07-27

Variant appearance in text: rs3774937
PubMed Link: 36011257
Variant Present in the following documents:
  • Main text
  • genes-13-01343.pdf
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A systems genomics approach to uncover patient-specific pathogenic pathways and proteins in ulcerative colitis.

Nature Communications
Brooks-Warburton, Johanne J; Modos, Dezso D; Sudhakar, Padhmanand P; Madgwick, Matthew M; Thomas, John P JP; Bohar, Balazs B; Fazekas, David D; Zoufir, Azedine A; Kapuy, Orsolya O; Szalay-Beko, Mate M; Verstockt, Bram B; Hall, Lindsay J LJ; Watson, Alastair A; Tremelling, Mark M; Parkes, Miles M; Vermeire, Severine S; Bender, Andreas A; Carding, Simon R SR; Korcsmaros, Tamas T
Publication Date: 2022-04-28

Variant appearance in text: rs3774937
PubMed Link: 35484353
Variant Present in the following documents:
  • Main text
  • 41467_2022_Article_29998.pdf
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Association between NF-κB Signal Pathway-Related Gene Polymorphisms and Response to Alendronate Treatment in Postmenopausal Chinese Women with Low Bone Mineral Density.

Evidence-Based Complementary And Alternative Medicine : Ecam
Shen, Xiaoyi X; Tan, Sasa S; Feng, Xianzhen X; Fu, Wenzhen W; Hu, Yunqiu Y; Li, Miao M; Wang, Wenjie W; Yuan, Hu H; Liu, Li L; Wang, Chun C; Hua, Fei F
Publication Date: 2022

Variant appearance in text: rs3774937
PubMed Link: 35368772
Variant Present in the following documents:
  • ECAM2022-2461716.pdf
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Linkage analysis identifies novel genetic modifiers of microbiome traits in families with inflammatory bowel disease.

Gut Microbes
Sharma, Arunabh A; Szymczak, Silke S; Rühlemann, Malte M; Freitag-Wolf, Sandra S; Knecht, Carolin C; Enderle, Janna J; Schreiber, Stefan S; Franke, Andre A; Lieb, Wolfgang W; Krawczak, Michael M; Dempfle, Astrid A
Publication Date: 2022

Variant appearance in text: rs3774937
PubMed Link: 35129060
Variant Present in the following documents:
  • Main text
  • KGMI_14_2024415.pdf
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Linkage analysis identifies novel genetic modifiers of microbiome traits in families with inflammatory bowel disease.

Gut Microbes
Sharma, Arunabh A; Szymczak, Silke S; Rühlemann, Malte M; Freitag-Wolf, Sandra S; Knecht, Carolin C; Enderle, Janna J; Schreiber, Stefan S; Franke, Andre A; Lieb, Wolfgang W; Krawczak, Michael M; Dempfle, Astrid A
Publication Date: 2022

Variant appearance in text: rs3774937
PubMed Link: 35129060
Variant Present in the following documents:
  • Main text
  • KGMI_14_2024415.pdf
View BVdb publication page



Association between NF-kB polymorphism and age-related macular degeneration in a high-altitude population.

Plos One
Xin, Yan Y; Zefeng, Kang K; Ling, Li L; Ruijuan, Guan G
Publication Date: 2021

Variant appearance in text: rs3774937
PubMed Link: 34101738
Variant Present in the following documents:
  • Main text
  • pone.0251931.pdf
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Genetic impacts on DNA methylation: research findings and future perspectives.

Genome Biology
Villicaña, Sergio S; Bell, Jordana T JT
Publication Date: 2021-04-30

Variant appearance in text: rs3774937
PubMed Link: 33931130
Variant Present in the following documents:
  • Main text
View BVdb publication page



Germline Genetic Variants of Viral Entry and Innate Immunity May Influence Susceptibility to SARS-CoV-2 Infection: Toward a Polygenic Risk Score for Risk Stratification.

Frontiers In Immunology
Grolmusz, Vince Kornél VK; Bozsik, Anikó A; Papp, János J; Patócs, Attila A
Publication Date: 2021

Variant appearance in text: rs3774937
PubMed Link: 33763088
Variant Present in the following documents:
  • Main text
  • fimmu-12-653489.pdf
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Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03

Variant appearance in text: rs3774937
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
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The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis.

Nature Communications
Xie, Jingyuan J; Liu, Lili L; Mladkova, Nikol N; Li, Yifu Y; Ren, Hong H; Wang, Weiming W; Cui, Zhao Z; Lin, Li L; Hu, Xiaofan X; Yu, Xialian X; Xu, Jing J; Liu, Gang G; Caliskan, Yasar Y; Sidore, Carlo C; Balderes, Olivia O; Rosen, Raphael J RJ; Bodria, Monica M; Zanoni, Francesca F; Zhang, Jun Y JY; Krithivasan, Priya P; Mehl, Karla K; Marasa, Maddalena M; Khan, Atlas A; Ozay, Fatih F; Canetta, Pietro A PA; Bomback, Andrew S AS; Appel, Gerald B GB; Sanna-Cherchi, Simone S; Sampson, Matthew G MG; Mariani, Laura H LH; Perkowska-Ptasinska, Agnieszka A; Durlik, Magdalena M; Mucha, Krzysztof K; Moszczuk, Barbara B; Foroncewicz, Bartosz B; Pączek, Leszek L; Habura, Ireneusz I; Ars, Elisabet E; Ballarin, Jose J; Mani, Laila-Yasmin LY; Vogt, Bruno B; Ozturk, Savas S; Yildiz, Abdülmecit A; Seyahi, Nurhan N; Arikan, Hakki H; Koc, Mehmet M; Basturk, Taner T; Karahan, Gonca G; Akgul, Sebahat Usta SU; Sever, Mehmet Sukru MS; Zhang, Dan D; Santoro, Domenico D; Bonomini, Mario M; Londrino, Francesco F; Gesualdo, Loreto L; Reiterova, Jana J; Tesar, Vladimir V; Izzi, Claudia C; Savoldi, Silvana S; Spotti, Donatella D; Marcantoni, Carmelita C; Messa, Piergiorgio P; Galliani, Marco M; Roccatello, Dario D; Granata, Simona S; Zaza, Gianluigi G; Lugani, Francesca F; Ghiggeri, GianMarco G; Pisani, Isabella I; Allegri, Landino L; Sprangers, Ben B; Park, Jin-Ho JH; Cho, BeLong B; Kim, Yon Su YS; Kim, Dong Ki DK; Suzuki, Hitoshi H; Amoroso, Antonio A; Cattran, Daniel C DC; Fervenza, Fernando C FC; Pani, Antonello A; Hamilton, Patrick P; Harris, Shelly S; Gupta, Sanjana S; Cheshire, Chris C; Dufek, Stephanie S; Issler, Naomi N; Pepper, Ruth J RJ; Connolly, John J; Powis, Stephen S; Bockenhauer, Detlef D; Stanescu, Horia C HC; Ashman, Neil N; Loos, Ruth J F RJF; Kenny, Eimear E EE; Wuttke, Matthias M; Eckardt, Kai-Uwe KU; Köttgen, Anna A; Hofstra, Julia M JM; Coenen, Marieke J H MJH; Kiemeney, Lambertus A LA; Akilesh, Shreeram S; Kretzler, Matthias M; Beck, Lawrence H LH; Stengel, Benedicte B; Debiec, Hanna H; Ronco, Pierre P; Wetzels, Jack F M JFM; Zoledziewska, Magdalena M; Cucca, Francesco F; Ionita-Laza, Iuliana I; Lee, Hajeong H; Hoxha, Elion E; Stahl, Rolf A K RAK; Brenchley, Paul P; Scolari, Francesco F; Zhao, Ming-Hui MH; Gharavi, Ali G AG; Kleta, Robert R; Chen, Nan N; Kiryluk, Krzysztof K
Publication Date: 2020-03-30

Variant appearance in text: rs3774937
PubMed Link: 32231244
Variant Present in the following documents:
  • 41467_2020_15383_MOESM1_ESM.pdf
View BVdb publication page



Inferring Interaction Networks From Multi-Omics Data.

Frontiers In Genetics
Hawe, Johann S JS; Theis, Fabian J FJ; Heinig, Matthias M
Publication Date: 2019

Variant appearance in text: rs3774937
PubMed Link: 31249591
Variant Present in the following documents:
  • Main text
  • fgene-10-00535.pdf
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Three-Dimensional Magnetic Resonance Imaging Reveals the Relationship Between the Control of Vertigo and Decreases in Endolymphatic Hydrops After Endolymphatic Sac Drainage With Steroids for Meniere's Disease.

Frontiers In Neurology
Ito, Taeko T; Inui, Hiroshi H; Miyasaka, Toshiteru T; Shiozaki, Tomoyuki T; Matsuyama, Shohei S; Yamanaka, Toshiaki T; Kichikawa, Kimihiko K; Takeda, Noriaki N; Kitahara, Tadashi T
Publication Date: 2019

Variant appearance in text: rs3774937
PubMed Link: 30778329
Variant Present in the following documents:
  • Main text
  • fneur-10-00046.pdf
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NFKB1 and MANBA Confer Disease Susceptibility to Primary Biliary Cholangitis via Independent Putative Primary Functional Variants.

Cellular And Molecular Gastroenterology And Hepatology
Hitomi, Yuki Y; Nakatani, Ken K; Kojima, Kaname K; Nishida, Nao N; Kawai, Yosuke Y; Kawashima, Minae M; Aiba, Yoshihiro Y; Nagasaki, Masao M; Nakamura, Minoru M; Tokunaga, Katsushi K
Publication Date: 2019

Variant appearance in text: rs3774937
PubMed Link: 30528300
Variant Present in the following documents:
  • Main text
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Towards personalized medicine in Ménière's disease.

F1000Research
Lopez-Escamez, Jose Antonio JA; Batuecas-Caletrio, Angel A; Bisdorff, Alexandre A
Publication Date: 2018

Variant appearance in text: rs3774937
PubMed Link: 30430003
Variant Present in the following documents:
  • Main text
  • f1000research-7-15693.pdf
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Graft versus Host Disease: From Basic Pathogenic Principles to DNA Damage Response and Cellular Senescence.

Mediators Of Inflammation
Kuba, Adam A; Raida, Ludek L
Publication Date: 2018

Variant appearance in text: rs3774937
PubMed Link: 29785172
Variant Present in the following documents:
  • Main text
  • MI2018-9451950.pdf
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Post-genomic behavioral genetics: From revolution to routine.

Genes, Brain, And Behavior
Ashbrook, D G DG; Mulligan, M K MK; Williams, R W RW
Publication Date: 2018-03

Variant appearance in text: rs3774937
PubMed Link: 29193773
Variant Present in the following documents:
  • Main text
View BVdb publication page



Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Publication Date: 2017-05-12

Variant appearance in text: rs3774937
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



A genome wide association study identifies a lncRna as risk factor for pathological inflammatory responses in leprosy.

Plos Genetics
Fava, Vinicius M VM; Manry, Jeremy J; Cobat, Aurélie A; Orlova, Marianna M; Van Thuc, Nguyen N; Moraes, Milton O MO; Sales-Marques, Carolinne C; Stefani, Mariane M A MM; Latini, Ana Carla P AC; Belone, Andrea F AF; Thai, Vu Hong VH; Abel, Laurent L; Alcaïs, Alexandre A; Schurr, Erwin E
Publication Date: 2017-02

Variant appearance in text: rs3774937
PubMed Link: 28222097
Variant Present in the following documents:
  • Main text
View BVdb publication page



Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci.

Nature Genetics
Ellinghaus, David D; Jostins, Luke L; Spain, Sarah L SL; Cortes, Adrian A; Bethune, Jörn J; Han, Buhm B; Park, Yu Rang YR; Raychaudhuri, Soumya S; Pouget, Jennie G JG; Hübenthal, Matthias M; Folseraas, Trine T; Wang, Yunpeng Y; Esko, Tonu T; Metspalu, Andres A; Westra, Harm-Jan HJ; Franke, Lude L; Pers, Tune H TH; Weersma, Rinse K RK; Collij, Valerie V; D'Amato, Mauro M; Halfvarson, Jonas J; Jensen, Anders Boeck AB; Lieb, Wolfgang W; Degenhardt, Franziska F; Forstner, Andreas J AJ; Hofmann, Andrea A; , ; , ; , ; , ; , ; Schreiber, Stefan S; Mrowietz, Ulrich U; Juran, Brian D BD; Lazaridis, Konstantinos N KN; Brunak, Søren S; Dale, Anders M AM; Trembath, Richard C RC; Weidinger, Stephan S; Weichenthal, Michael M; Ellinghaus, Eva E; Elder, James T JT; Barker, Jonathan N W N JN; Andreassen, Ole A OA; McGovern, Dermot P DP; Karlsen, Tom H TH; Barrett, Jeffrey C JC; Parkes, Miles M; Brown, Matthew A MA; Franke, Andre A
Publication Date: 2016-05

Variant appearance in text: rs3774937
PubMed Link: 26974007
Variant Present in the following documents:
  • Main text
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Candidate gene association studies and risk of Hodgkin lymphoma: a systematic review and meta-analysis.

Hematological Oncology
Sud, Amit A; Hemminki, Kari K; Houlston, Richard S RS
Publication Date: 2017-03

Variant appearance in text: rs3774937
PubMed Link: 26053036
Variant Present in the following documents:
  • Main text
View BVdb publication page



Physicians abstracts.

Bone Marrow Transplantation
Publication Date: 2015-03

Variant appearance in text: rs3774937
PubMed Link: 25794251
Variant Present in the following documents:
  • 41409_2015_Article_BFbmt201527.pdf
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Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease.

Plos One
Cabrera, Sonia S; Sanchez, Elena E; Requena, Teresa T; Martinez-Bueno, Manuel M; Benitez, Jesus J; Perez, Nicolas N; Trinidad, Gabriel G; Soto-Varela, Andrés A; Santos-Perez, Sofía S; Martin-Sanz, Eduardo E; Fraile, Jesus J; Perez, Paz P; Alarcon-Riquelme, Marta E ME; Batuecas, Angel A; Espinosa-Sanchez, Juan M JM; Aran, Ismael I; Lopez-Escamez, Jose A JA
Publication Date: 2014

Variant appearance in text: rs3774937
PubMed Link: 25397881
Variant Present in the following documents:
  • Main text
  • pone.0112171.pdf
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Genetic variants in fas signaling pathway genes and risk of gastric cancer.

International Journal Of Cancer
Hyland, Paula L PL; Lin, Shih-Wen SW; Hu, Nan N; Zhang, Han H; Wang, Lemin L; Su, Hua H; Wang, Chaoyu C; Ding, Ti T; Tang, Ze-Zhong ZZ; Fan, Jin-Hu JH; Qiao, You-Lin YL; Xiong, Xiaoqin X; Wheeler, William W; Giffen, Carol C; Yu, Kai K; Yuenger, Jeff J; Burdett, Laurie L; Wang, Zhaoming Z; Chanock, Stephen J SJ; Tucker, Margaret A MA; Dawsey, Sanford M SM; Freedman, Neal D ND; Goldstein, Alisa M AM; Abnet, Christian C CC; Taylor, Philip R PR
Publication Date: 2014-02-15

Variant appearance in text: rs3774937
PubMed Link: 23921907
Variant Present in the following documents:
  • Main text
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Pathway-Targeted Pharmacogenomics of CYP1A2 in Human Liver.

Frontiers In Pharmacology
Klein, Kathrin K; Winter, Stefan S; Turpeinen, Miia M; Schwab, Matthias M; Zanger, Ulrich M UM
Publication Date: 2010

Variant appearance in text: rs3774937
PubMed Link: 21918647
Variant Present in the following documents:
  • Main text
  • fphar-01-00129.pdf
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Polymorphic variation in NFKB1 and other aspirin-related genes and risk of Hodgkin lymphoma.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Chang, Ellen T ET; Birmann, Brenda M BM; Kasperzyk, Julie L JL; Conti, David V DV; Kraft, Peter P; Ambinder, Richard F RF; Zheng, Tongzhang T; Mueller, Nancy E NE
Publication Date: 2009-03

Variant appearance in text: rs3774937
PubMed Link: 19223558
Variant Present in the following documents:
  • Main text
View BVdb publication page