FGFR2 c.110-13757T>C

Variant ID: 10-123338975-A-G

NM_000141.4(FGFR2):c.110-13757T>C

This variant was identified in 18 publications

View GRCh38 version.




Publications:


FinnGen provides genetic insights from a well-phenotyped isolated population.

Nature
Kurki, Mitja I MI; Karjalainen, Juha J; Palta, Priit P; Sipilä, Timo P TP; Kristiansson, Kati K; Donner, Kati M KM; Reeve, Mary P MP; Laivuori, Hannele H; Aavikko, Mervi M; Kaunisto, Mari A MA; Loukola, Anu A; Lahtela, Elisa E; Mattsson, Hannele H; Laiho, Päivi P; Della Briotta Parolo, Pietro P; Lehisto, Arto A AA; Kanai, Masahiro M; Mars, Nina N; Rämö, Joel J; Kiiskinen, Tuomo T; Heyne, Henrike O HO; Veerapen, Kumar K; Rüeger, Sina S; Lemmelä, Susanna S; Zhou, Wei W; Ruotsalainen, Sanni S; Pärn, Kalle K; Hiekkalinna, Tero T; Koskelainen, Sami S; Paajanen, Teemu T; Llorens, Vincent V; Gracia-Tabuenca, Javier J; Siirtola, Harri H; Reis, Kadri K; Elnahas, Abdelrahman G AG; Sun, Benjamin B; Foley, Christopher N CN; Aalto-Setälä, Katriina K; Alasoo, Kaur K; Arvas, Mikko M; Auro, Kirsi K; Biswas, Shameek S; Bizaki-Vallaskangas, Argyro A; Carpen, Olli O; Chen, Chia-Yen CY; Dada, Oluwaseun A OA; Ding, Zhihao Z; Ehm, Margaret G MG; Eklund, Kari K; Färkkilä, Martti M; Finucane, Hilary H; Ganna, Andrea A; Ghazal, Awaisa A; Graham, Robert R RR; Green, Eric M EM; Hakanen, Antti A; Hautalahti, Marco M; Hedman, Åsa K ÅK; Hiltunen, Mikko M; Hinttala, Reetta R; Hovatta, Iiris I; Hu, Xinli X; Huertas-Vazquez, Adriana A; Huilaja, Laura L; Hunkapiller, Julie J; Jacob, Howard H; Jensen, Jan-Nygaard JN; Joensuu, Heikki H; John, Sally S; Julkunen, Valtteri V; Jung, Marc M; Junttila, Juhani J; Kaarniranta, Kai K; Kähönen, Mika M; Kajanne, Risto R; Kallio, Lila L; Kälviäinen, Reetta R; Kaprio, Jaakko J; , ; Kerimov, Nurlan N; Kettunen, Johannes J; Kilpeläinen, Elina E; Kilpi, Terhi T; Klinger, Katherine K; Kosma, Veli-Matti VM; Kuopio, Teijo T; Kurra, Venla V; Laisk, Triin T; Laukkanen, Jari J; Lawless, Nathan N; Liu, Aoxing A; Longerich, Simonne S; Mägi, Reedik R; Mäkelä, Johanna J; Mäkitie, Antti A; Malarstig, Anders A; Mannermaa, Arto A; Maranville, Joseph J; Matakidou, Athena A; Meretoja, Tuomo T; Mozaffari, Sahar V SV; Niemi, Mari E K MEK; Niemi, Marianna M; Niiranen, Teemu T; O Donnell, Christopher J CJ; Obeidat, Ma En ME; Okafo, George G; Ollila, Hanna M HM; Palomäki, Antti A; Palotie, Tuula T; Partanen, Jukka J; Paul, Dirk S DS; Pelkonen, Margit M; Pendergrass, Rion K RK; Petrovski, Slavé S; Pitkäranta, Anne A; Platt, Adam A; Pulford, David D; Punkka, Eero E; Pussinen, Pirkko P; Raghavan, Neha N; Rahimov, Fedik F; Rajpal, Deepak D; Renaud, Nicole A NA; Riley-Gillis, Bridget B; Rodosthenous, Rodosthenis R; Saarentaus, Elmo E; Salminen, Aino A; Salminen, Eveliina E; Salomaa, Veikko V; Schleutker, Johanna J; Serpi, Raisa R; Shen, Huei-Yi HY; Siegel, Richard R; Silander, Kaisa K; Siltanen, Sanna S; Soini, Sirpa S; Soininen, Hilkka H; Sul, Jae Hoon JH; Tachmazidou, Ioanna I; Tasanen, Kaisa K; Tienari, Pentti P; Toppila-Salmi, Sanna S; Tukiainen, Taru T; Tuomi, Tiinamaija T; Turunen, Joni A JA; Ulirsch, Jacob C JC; Vaura, Felix F; Virolainen, Petri P; Waring, Jeffrey J; Waterworth, Dawn D; Yang, Robert R; Nelis, Mari M; Reigo, Anu A; Metspalu, Andres A; Milani, Lili L; Esko, Tõnu T; Fox, Caroline C; Havulinna, Aki S AS; Perola, Markus M; Ripatti, Samuli S; Jalanko, Anu A; Laitinen, Tarja T; Mäkelä, Tomi P TP; Plenge, Robert R; McCarthy, Mark M; Runz, Heiko H; Daly, Mark J MJ; Palotie, Aarno A
Publication Date: 2023-01

Variant appearance in text: rs1078806
PubMed Link: 36653562
Variant Present in the following documents:
  • 41586_2022_5473_MOESM4_ESM.xlsx, sheet 8
View BVdb publication page



Considering hormone-sensitive cancers as a single disease in the UK biobank reveals shared aetiology.

Communications Biology
Ahmed, Muktar M; Mäkinen, Ville-Petteri VP; Mulugeta, Anwar A; Shin, Jisu J; Boyle, Terry T; Hyppönen, Elina E; Lee, Sang Hong SH
Publication Date: 2022-06-21

Variant appearance in text: rs1078806
PubMed Link: 35729236
Variant Present in the following documents:
  • 42003_2022_3554_MOESM2_ESM.pdf
View BVdb publication page



Genes and Pathways Associated with Skeletal Sagittal Malocclusions: A Systematic Review.

International Journal Of Molecular Sciences
Gershater, Elizabeth E; Li, Chenshuang C; Ha, Pin P; Chung, Chun-Hsi CH; Tanna, Nipul N; Zou, Min M; Zheng, Zhong Z
Publication Date: 2021-12-02

Variant appearance in text: rs1078806
PubMed Link: 34884839
Variant Present in the following documents:
  • Main text
  • ijms-22-13037.pdf
View BVdb publication page



Genes and Pathways Associated with Skeletal Sagittal Malocclusions: A Systematic Review.

International Journal Of Molecular Sciences
Gershater, Elizabeth E; Li, Chenshuang C; Ha, Pin P; Chung, Chun-Hsi CH; Tanna, Nipul N; Zou, Min M; Zheng, Zhong Z
Publication Date: 2021-12-02

Variant appearance in text: rs1078806
PubMed Link: 34884839
Variant Present in the following documents:
  • Main text
  • ijms-22-13037.pdf
View BVdb publication page



A sequential methodology for the rapid identification and characterization of breast cancer-associated functional SNPs.

Nature Communications
Zhao, Yihan Y; Wu, Di D; Jiang, Danli D; Zhang, Xiaoyu X; Wu, Ting T; Cui, Jing J; Qian, Min M; Zhao, Jean J; Oesterreich, Steffi S; Sun, Wei W; Finkel, Toren T; Li, Gang G
Publication Date: 2020-07-03

Variant appearance in text: rs1078806
PubMed Link: 32620845
Variant Present in the following documents:
  • 41467_2020_Article_17159.pdf
View BVdb publication page



FGFs/FGFRs-dependent signalling in regulation of steroid hormone receptors - implications for therapy of luminal breast cancer.

Journal Of Experimental & Clinical Cancer Research : Cr
Piasecka, Dominika D; Braun, Marcin M; Kitowska, Kamila K; Mieczkowski, Kamil K; Kordek, Radzislaw R; Sadej, Rafal R; Romanska, Hanna H
Publication Date: 2019-05-29

Variant appearance in text: rs1078806
PubMed Link: 31142340
Variant Present in the following documents:
  • Main text
  • 13046_2019_Article_1236.pdf
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The association of genetic variants in FGFR2 with osteoporosis susceptibility in Chinese Han population.

Bioscience Reports
Yang, Yang Y; Fei, Mengxue M; Zhou, Xinying X; Li, Yuejun Y; Jin, Dadi D
Publication Date: 2019-06-28

Variant appearance in text: rs1078806
PubMed Link: 31113874
Variant Present in the following documents:
  • Main text
View BVdb publication page



Fibroblast Growth Factor Receptor 2 Signaling in Breast Cancer.

International Journal Of Biological Sciences
Lei, Haipeng H; Deng, Chu-Xia CX
Publication Date: 2017

Variant appearance in text: rs1078806
PubMed Link: 29104507
Variant Present in the following documents:
  • Main text
  • ijbsv13p1163.pdf
View BVdb publication page



FGF-2 Gene Polymorphism in Osteoporosis among Guangxi's Zhuang Chinese.

International Journal Of Molecular Sciences
Bin, Xiaoyun X; Lin, Chaowen C; Huang, Xiufeng X; Zhou, Qinghui Q; Wang, Liping L; Xian, Cory J CJ
Publication Date: 2017-06-27

Variant appearance in text: rs1078806
PubMed Link: 28653999
Variant Present in the following documents:
  • Main text
  • ijms-18-01358.pdf
View BVdb publication page



Heterogeneity of Breast Cancer Associations with Common Genetic Variants in FGFR2 according to the Intrinsic Subtypes in Southern Han Chinese Women.

Biomed Research International
Liang, Huiying H; Yang, Xuexi X; Chen, Lujia L; Li, Hong H; Zhu, Anna A; Sun, Minying M; Wang, Haitao H; Li, Ming M
Publication Date: 2015

Variant appearance in text: rs1078806
PubMed Link: 26421298
Variant Present in the following documents:
  • Main text
View BVdb publication page



Using parental phenotypes in case-parent studies.

Frontiers In Genetics
Shi, Min M; Umbach, David M DM; Weinberg, Clarice R CR
Publication Date: 2015

Variant appearance in text: rs1078806
PubMed Link: 26157456
Variant Present in the following documents:
  • Main text
  • fgene-06-00221.pdf
View BVdb publication page



Replication of breast cancer susceptibility loci in whites and African Americans using a Bayesian approach.

American Journal Of Epidemiology
O'Brien, Katie M KM; Cole, Stephen R SR; Poole, Charles C; Bensen, Jeannette T JT; Herring, Amy H AH; Engel, Lawrence S LS; Millikan, Robert C RC
Publication Date: 2014-02-01

Variant appearance in text: rs1078806
PubMed Link: 24218030
Variant Present in the following documents:
  • Main text
View BVdb publication page



Breast cancer subtypes and previously established genetic risk factors: a bayesian approach.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
O'Brien, Katie M KM; Cole, Stephen R SR; Engel, Lawrence S LS; Bensen, Jeannette T JT; Poole, Charles C; Herring, Amy H AH; Millikan, Robert C RC
Publication Date: 2014-01

Variant appearance in text: rs1078806
PubMed Link: 24177593
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation.

Human Genetics
Rinella, Erica S ES; Shao, Yongzhao Y; Yackowski, Lauren L; Pramanik, Sreemanta S; Oratz, Ruth R; Schnabel, Freya F; Guha, Saurav S; LeDuc, Charles C; Campbell, Christopher L CL; Klugman, Susan D SD; Terry, Mary Beth MB; Senie, Ruby T RT; Andrulis, Irene L IL; Daly, Mary M; John, Esther M EM; Roses, Daniel D; Chung, Wendy K WK; Ostrer, Harry H
Publication Date: 2013-05

Variant appearance in text: rs1078806
PubMed Link: 23354978
Variant Present in the following documents:
  • Main text
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An integrative genomics approach to biomarker discovery in breast cancer.

Cancer Informatics
Hicks, Chindo C; Asfour, Rozana R; Pannuti, Antonio A; Miele, Lucio L
Publication Date: 2011

Variant appearance in text: rs1078806
PubMed Link: 21869864
Variant Present in the following documents:
  • Main text
  • cin-10-2011-185.pdf
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Relation of FGFR2 genetic polymorphisms to the association between oral contraceptive use and the risk of breast cancer in Chinese women.

American Journal Of Epidemiology
Xu, Wang-Hong WH; Shu, Xiao-Ou XO; Long, Jirong J; Lu, Wei W; Cai, Qiuyin Q; Zheng, Ying Y; Xiang, Yong-Bing YB; Dai, Qi Q; Zhao, Gen-Ming GM; Gu, Kai K; Bao, Ping-Ping PP; Gao, Yu-Tang YT; Zheng, Wei W
Publication Date: 2011-04-15

Variant appearance in text: rs1078806
PubMed Link: 21382839
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association studies of cancer.

Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology
Stadler, Zsofia K ZK; Thom, Peter P; Robson, Mark E ME; Weitzel, Jeffrey N JN; Kauff, Noah D ND; Hurley, Karen E KE; Devlin, Vincent V; Gold, Bert B; Klein, Robert J RJ; Offit, Kenneth K
Publication Date: 2010-09-20

Variant appearance in text: rs1078806
PubMed Link: 20585100
Variant Present in the following documents:
  • Main text
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A risk variant in an miR-125b binding site in BMPR1B is associated with breast cancer pathogenesis.

Cancer Research
Saetrom, Pål P; Biesinger, Jacob J; Li, Sierra M SM; Smith, David D; Thomas, Laurent F LF; Majzoub, Karim K; Rivas, Guillermo E GE; Alluin, Jessica J; Rossi, John J JJ; Krontiris, Theodore G TG; Weitzel, Jeffrey J; Daly, Mary B MB; Benson, Al B AB; Kirkwood, John M JM; O'Dwyer, Peter J PJ; Sutphen, Rebecca R; Stewart, James A JA; Johnson, David D; Larson, Garrett P GP
Publication Date: 2009-09-15

Variant appearance in text: rs1078806
PubMed Link: 19738052
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Gold, Bert B; Kirchhoff, Tomas T; Stefanov, Stefan S; Lautenberger, James J; Viale, Agnes A; Garber, Judy J; Friedman, Eitan E; Narod, Steven S; Olshen, Adam B AB; Gregersen, Peter P; Kosarin, Kristi K; Olsh, Adam A; Bergeron, Julie J; Ellis, Nathan A NA; Klein, Robert J RJ; Clark, Andrew G AG; Norton, Larry L; Dean, Michael M; Boyd, Jeff J; Offit, Kenneth K
Publication Date: 2008-03-18

Variant appearance in text: rs1078806
PubMed Link: 18326623
Variant Present in the following documents:
  • Main text
View BVdb publication page