TGFB1 c.356-174A>T

Variant ID: 19-41854534-T-A

NM_000660.4(TGFB1):c.356-174A>T

This variant was identified in 12 publications

View GRCh38 version.




Publications:


Genetic Factors for Coronary Heart Disease and Their Mechanisms: A Meta-Analysis and Comprehensive Review of Common Variants from Genome-Wide Association Studies.

Diagnostics (Basel, Switzerland)
Zarkasi, Khairul Anwar KA; Abdullah, Noraidatulakma N; Abdul Murad, Nor Azian NA; Ahmad, Norfazilah N; Jamal, Rahman R
Publication Date: 2022-10-21

Variant appearance in text: rs8108632
PubMed Link: 36292250
Variant Present in the following documents:
  • diagnostics-12-02561.pdf
View BVdb publication page



Polygenic risk for coronary artery disease in the Scottish and English population.

Bmc Cardiovascular Disorders
Yang, Chuhua C; Starnecker, Fabian F; Pang, Shichao S; Chen, Zhifen Z; Güldener, Ulrich U; Li, Ling L; Heinig, Matthias M; Schunkert, Heribert H
Publication Date: 2021-12-07

Variant appearance in text: rs8108632
PubMed Link: 34876023
Variant Present in the following documents:
  • 12872_2021_2398_MOESM1_ESM.pdf
View BVdb publication page



Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control.

Diabetologia
Tremblay, Johanne J; Haloui, Mounsif M; Attaoua, Redha R; Tahir, Ramzan R; Hishmih, Camil C; Harvey, François F; Marois-Blanchet, François-Christophe FC; Long, Carole C; Simon, Paul P; Santucci, Lara L; Hizel, Candan C; Chalmers, John J; Marre, Michel M; Harrap, Stephen S; Cífková, Renata R; Krajčoviechová, Alena A; Matthews, David R DR; Williams, Bryan B; Poulter, Neil N; Zoungas, Sophia S; Colagiuri, Stephen S; Mancia, Giuseppe G; Grobbee, Diederick E DE; Rodgers, Anthony A; Liu, Liusheng L; Agbessi, Mawussé M; Bruat, Vanessa V; Favé, Marie-Julie MJ; Harwood, Michelle P MP; Awadalla, Philip P; Woodward, Mark M; Hussin, Julie G JG; Hamet, Pavel P
Publication Date: 2021-09

Variant appearance in text: rs8108632
PubMed Link: 34226943
Variant Present in the following documents:
  • 125_2021_5491_MOESM1_ESM.pdf
View BVdb publication page



Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells.

Circulation Research
Aherrahrou, Redouane R; Guo, Liang L; Nagraj, V Peter VP; Aguhob, Aaron A; Hinkle, Jameson J; Chen, Lisa L; Yuhl Soh, Joon J; Lue, Dillon D; Alencar, Gabriel F GF; Boltjes, Arjan A; van der Laan, Sander W SW; Farber, Emily E; Fuller, Daniela D; Anane-Wae, Rita R; Akingbesote, Ngozi N; Manichaikul, Ani W AW; Ma, Lijiang L; Kaikkonen, Minna U MU; Björkegren, Johan L M JLM; Önengüt-Gümüşcü, Suna S; Pasterkamp, Gerard G; Miller, Clint L CL; Owens, Gary K GK; Finn, Aloke A; Navab, Mohamad M; Fogelman, Alan M AM; Berliner, Judith A JA; Civelek, Mete M
Publication Date: 2020-12-04

Variant appearance in text: rs8108632
PubMed Link: 33040646
Variant Present in the following documents:
  • Main text
View BVdb publication page



A Single-Nucleotide Polymorphism (rs1131243) of the Transforming Growth Factor Beta Signaling Pathway Contributes to Risk of Acute Rejection in Chinese Renal Transplant Recipients.

Medical Science Monitor : International Medical Journal Of Experimental And Clinical Research
Zheng, Ming M; Yang, Haiwei H; Li, Wencheng W; Zhou, Jiajun J; Wei, Jintao J; Wang, Zijie Z; Guo, Miao M; Chen, Hao H; Sun, Li L; Han, Zhijian Z; Tao, Jun J; Ju, Xiaobing X; Tan, Ruoyun R; Wei, Jifu J; Gu, Min M
Publication Date: 2019-12-01

Variant appearance in text: rs8108632
PubMed Link: 31786580
Variant Present in the following documents:
  • Main text
  • medscimonit-25-9138.pdf
View BVdb publication page



Genome-Wide Association Studies of Hypertension and Several Other Cardiovascular Diseases.

Pulse (Basel, Switzerland)
Wang, Yan Y; Wang, Ji-Guang JG
Publication Date: 2019-04

Variant appearance in text: rs8108632
PubMed Link: 31049317
Variant Present in the following documents:
  • Main text
View BVdb publication page



Tissue-specific Network Analysis of Genetic Variants Associated with Coronary Artery Disease.

Scientific Reports
Miao, Xiao X; Chen, Xinlin X; Xie, Zhijun Z; Lin, Honghuang H
Publication Date: 2018-07-31

Variant appearance in text: rs8108632
PubMed Link: 30065343
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_29904.pdf
View BVdb publication page



Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.

Cardiovascular Diabetology
Charmet, Romain R; Duffy, Seamus S; Keshavarzi, Sareh S; Gyorgy, Beata B; Marre, Michel M; Rossing, Peter P; McKnight, Amy Jayne AJ; Maxwell, Alexander P AP; Ahluwalia, Tarun Veer Singh TVS; Paterson, Andrew D AD; Trégouët, David-Alexandre DA; Hadjadj, Samy S
Publication Date: 2018-04-25

Variant appearance in text: rs8108632
PubMed Link: 29695241
Variant Present in the following documents:
  • Main text
  • 12933_2018_Article_705.pdf
View BVdb publication page



Genetic Associations with Gestational Duration and Spontaneous Preterm Birth.

The New England Journal Of Medicine
Zhang, Ge G; Feenstra, Bjarke B; Bacelis, Jonas J; Liu, Xueping X; Muglia, Lisa M LM; Juodakis, Julius J; Miller, Daniel E DE; Litterman, Nadia N; Jiang, Pan-Pan PP; Russell, Laura L; Hinds, David A DA; Hu, Youna Y; Weirauch, Matthew T MT; Chen, Xiaoting X; Chavan, Arun R AR; Wagner, Günter P GP; Pavličev, Mihaela M; Nnamani, Mauris C MC; Maziarz, Jamie J; Karjalainen, Minna K MK; Rämet, Mika M; Sengpiel, Verena V; Geller, Frank F; Boyd, Heather A HA; Palotie, Aarno A; Momany, Allison A; Bedell, Bruce B; Ryckman, Kelli K KK; Huusko, Johanna M JM; Forney, Carmy R CR; Kottyan, Leah C LC; Hallman, Mikko M; Teramo, Kari K; Nohr, Ellen A EA; Davey Smith, George G; Melbye, Mads M; Jacobsson, Bo B; Muglia, Louis J LJ
Publication Date: 2017-09-21

Variant appearance in text: rs8108632
PubMed Link: 28877031
Variant Present in the following documents:
  • NEJMoa1612665-Muglia-Supplement.pdf
View BVdb publication page



Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease.

Nature Genetics
Klarin, Derek D; Zhu, Qiuyu Martin QM; Emdin, Connor A CA; Chaffin, Mark M; Horner, Steven S; McMillan, Brian J BJ; Leed, Alison A; Weale, Michael E ME; Spencer, Chris C A CCA; Aguet, François F; Segrè, Ayellet V AV; Ardlie, Kristin G KG; Khera, Amit V AV; Kaushik, Virendar K VK; Natarajan, Pradeep P; , ; Kathiresan, Sekar S
Publication Date: 2017-09

Variant appearance in text: rs8108632
PubMed Link: 28714974
Variant Present in the following documents:
  • Main text
  • NIHMS885618-supplement-4.xlsx, sheet 1
View BVdb publication page



Identification of 15 novel risk loci for coronary artery disease and genetic risk of recurrent events, atrial fibrillation and heart failure.

Scientific Reports
Verweij, Niek N; Eppinga, Ruben N RN; Hagemeijer, Yanick Y; van der Harst, Pim P
Publication Date: 2017-06-05

Variant appearance in text: rs8108632
PubMed Link: 28584231
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_3062.pdf
  • 41598_2017_3062_MOESM1_ESM.pdf
View BVdb publication page



Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk.

Nature Genetics
Zhang, Ben B; Jia, Wei-Hua WH; Matsuda, Koichi K; Kweon, Sun-Seog SS; Matsuo, Keitaro K; Xiang, Yong-Bing YB; Shin, Aesun A; Jee, Sun Ha SH; Kim, Dong-Hyun DH; Cai, Qiuyin Q; Long, Jirong J; Shi, Jiajun J; Wen, Wanqing W; Yang, Gong G; Zhang, Yanfeng Y; Li, Chun C; Li, Bingshan B; Guo, Yan Y; Ren, Zefang Z; Ji, Bu-Tian BT; Pan, Zhi-Zhong ZZ; Takahashi, Atsushi A; Shin, Min-Ho MH; Matsuda, Fumihiko F; Gao, Yu-Tang YT; Oh, Jae Hwan JH; Kim, Soriul S; Ahn, Yoon-Ok YO; , ; Chan, Andrew T AT; Chang-Claude, Jenny J; Slattery, Martha L ML; , ; Gruber, Stephen B SB; Schumacher, Fredrick R FR; Stenzel, Stephanie L SL; , ; Casey, Graham G; Kim, Hyeong-Rok HR; Jeong, Jin-Young JY; Park, Ji Won JW; Li, Hong-Lan HL; Hosono, Satoyo S; Cho, Sang-Hee SH; Kubo, Michiaki M; Shu, Xiao-Ou XO; Zeng, Yi-Xin YX; Zheng, Wei W
Publication Date: 2014-06

Variant appearance in text: rs8108632
PubMed Link: 24836286
Variant Present in the following documents:
  • NIHMS588441-supplement-1.pdf
View BVdb publication page