ITGB3 c.*713A>G

Variant ID: 17-45388283-A-G

NM_000212.2(ITGB3):c.*713A>G

This variant was identified in 23 publications

View GRCh38 version.




Publications:


Impact of pharmacogenetics on aspirin resistance: a systematic review.

Arquivos De Neuro-Psiquiatria
Silva, Gustavo Figueiredo da GFD; Lopes, Bruno Mattei BM; Moser, Vinicius V; Ferreira, Leslie Ecker LE
Publication Date: 2023-01

Variant appearance in text: rs2317676
PubMed Link: 36918009
Variant Present in the following documents:
  • Main text
  • 10-1055-s-0042-1758445.pdf
View BVdb publication page



Inflammation and endothelial function relevant genetic polymorphisms in carotid stenosis in southwestern China.

Frontiers In Neurology
Liu, Lin L; Yi, Xingyang X; Luo, Hua H; Yu, Ming M
Publication Date: 2022

Variant appearance in text: rs2317676
PubMed Link: 36686520
Variant Present in the following documents:
  • Main text
  • fneur-13-1076898.pdf
View BVdb publication page



Association between P2Y1 and P2Y12 polymorphisms and acute myocardial infarction and ADP-induced platelet aggregation.

Bmc Cardiovascular Disorders
Su, Chunyan C; Zhang, Zhishan Z; Chen, Jintu J; Tian, Mengcha M; Wu, Conglian C; Zhang, Tao T
Publication Date: 2023-01-21

Variant appearance in text: rs2317676
PubMed Link: 36681816
Variant Present in the following documents:
  • 12872_2023_Article_3075.pdf
View BVdb publication page



MMP9 SNP and MMP SNP-SNP interactions increase the risk for ischemic stroke in the Han Hakka population.

Brain And Behavior
Fan, Daofeng D; Zheng, Chong C; Wu, Wenbao W; Chen, Yinjuan Y; Chen, Dongping D; Hu, Xiaohong X; Shen, Chaoxiong C; Chen, Mingsheng M; Li, Rongtong R; Chen, Yangui Y
Publication Date: 2022-02

Variant appearance in text: rs2317676
PubMed Link: 34984852
Variant Present in the following documents:
  • BRB3-12-e2473.pdf
View BVdb publication page



KLK3 SNP-SNP interactions for prediction of prostate cancer aggressiveness.

Scientific Reports
Lin, Hui-Yi HY; Huang, Po-Yu PY; Cheng, Chia-Ho CH; Tung, Heng-Yuan HY; Fang, Zhide Z; Berglund, Anders E AE; Chen, Ann A; French-Kwawu, Jennifer J; Harris, Darian D; Pow-Sang, Julio J; Yamoah, Kosj K; Cleveland, John L JL; Awasthi, Shivanshu S; Rounbehler, Robert J RJ; Gerke, Travis T; Dhillon, Jasreman J; Eeles, Rosalind R; Kote-Jarai, Zsofia Z; Muir, Kenneth K; , ; Schleutker, Johanna J; Pashayan, Nora N; , ; Neal, David E DE; Nielsen, Sune F SF; Nordestgaard, Børge G BG; Gronberg, Henrik H; Wiklund, Fredrik F; Giles, Graham G GG; Haiman, Christopher A CA; Travis, Ruth C RC; Stanford, Janet L JL; Kibel, Adam S AS; Cybulski, Cezary C; Khaw, Kay-Tee KT; Maier, Christiane C; Thibodeau, Stephen N SN; Teixeira, Manuel R MR; Cannon-Albright, Lisa L; Brenner, Hermann H; Kaneva, Radka R; Pandha, Hardev H; , ; Srinivasan, Srilakshmi S; Clements, Judith J; Batra, Jyotsna J; Park, Jong Y JY
Publication Date: 2021-04-29

Variant appearance in text: rs2317676
PubMed Link: 33927218
Variant Present in the following documents:
  • Main text
View BVdb publication page



Variants in clopidogrel-relevant genes and early neurological deterioration in ischemic stroke patients receiving clopidogrel.

Bmc Neurology
Yi, Xingyang X; Zhou, Qiang Q; Zhang, Yongyin Y; Zhou, Ju J; Lin, Jing J
Publication Date: 2020-04-28

Variant appearance in text: rs2317676
PubMed Link: 32345264
Variant Present in the following documents:
  • Main text
  • 12883_2020_Article_1703.pdf
View BVdb publication page



Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders
Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M
Publication Date: 2020-02-11

Variant appearance in text: rs2317676
PubMed Link: 32046637
Variant Present in the following documents:
  • 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: rs2317676
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



MicroRNA-binding site polymorphisms and risk of colorectal cancer: A systematic review and meta-analysis.

Cancer Medicine
Gholami, Morteza M; Larijani, Bagher B; Sharifi, Farshad F; Hasani-Ranjbar, Shirin S; Taslimi, Reza R; Bastami, Milad M; Atlasi, Rasha R; Amoli, Mahsa M MM
Publication Date: 2019-12

Variant appearance in text: rs2317676
PubMed Link: 31637880
Variant Present in the following documents:
  • Main text
  • CAM4-8-7477.pdf
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The TXA2R rs1131882, P2Y1 rs1371097 and GPIIIa rs2317676 three-loci interactions may increase the risk of carotid stenosis in patients with ischemic stroke.

Bmc Neurology
Yi, Xingyang X; Lin, Jing J; Zhou, Qiang Q; Huang, Ruyue R; Chai, Zhenxiao Z
Publication Date: 2019-03-26

Variant appearance in text: rs2317676
PubMed Link: 30914039
Variant Present in the following documents:
  • Main text
  • 12883_2019_Article_1271.pdf
View BVdb publication page



Platelet membrane receptor P2Y12 H1/H2 polymorphism is highly associated with cerebral infarction: a case-control study.

Neuropsychiatric Disease And Treatment
Lu, Shu-Jun SJ; Zhou, Xiao-Sheng XS; Zheng, Qi Q; Chen, Hong-Liang HL; Geng, Yan-Lei YL
Publication Date: 2018

Variant appearance in text: rs2317676
PubMed Link: 30214212
Variant Present in the following documents:
  • Main text
  • ndt-14-2225.pdf
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Interactions among variants in TXA2R, P2Y12 and GPIIIa are associated with carotid plaque vulnerability in Chinese population.

Oncotarget
Yi, Xingyang X; Lin, Jing J; Luo, Hua H; Zhou, Ju J; Zhou, Qiang Q; Wang, Yanfen Y; Wang, Chun C
Publication Date: 2018-04-03

Variant appearance in text: rs2317676
PubMed Link: 29707133
Variant Present in the following documents:
  • Main text
  • oncotarget-09-17597.pdf
View BVdb publication page



The polymorphisms of miRNA-binding site in MLH3 and ERCC1 were linked to the risk of colorectal cancer in a case-control study.

Cancer Medicine
Zhang, Qianye Q; Zheng, Xiao X; Li, Xiaoxia X; Sun, Deyu D; Xue, Ping P; Zhang, Guopei G; Xiao, Mingyang M; Cai, Yuan Y; Jin, Cuihong C; Yang, Jinghua J; Wu, Shengwen S; Lu, Xiaobo X
Publication Date: 2018-04

Variant appearance in text: rs2317676
PubMed Link: 29516665
Variant Present in the following documents:
  • Main text
  • CAM4-7-1264.pdf
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs2317676
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 1
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page



Interaction among CYP2C8, GPIIIa and P2Y12 variants increase susceptibility to ischemic stroke in Chinese population.

Oncotarget
Yi, Xingyang X; Lin, Jing J; Wang, Yanfen Y; Zhou, Ju J; Zhou, Qiang Q
Publication Date: 2017-09-19

Variant appearance in text: rs2317676
PubMed Link: 29050321
Variant Present in the following documents:
  • Main text
  • oncotarget-08-70811.pdf
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs2317676
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



Interactions among COX-2, GPIIIa and P2Y1 variants are associated with aspirin responsiveness and adverse events in patients with ischemic stroke.

Therapeutic Advances In Neurological Disorders
Yi, Xingyang X; Han, Zhao Z; Zhou, Qiang Q; Lin, Jing J; Wang, Chun C
Publication Date: 2017-03

Variant appearance in text: rs2317676
PubMed Link: 28344655
Variant Present in the following documents:
  • Main text
View BVdb publication page



Interaction among COX-2, P2Y1 and GPIIIa gene variants is associated with aspirin resistance and early neurological deterioration in Chinese stroke patients.

Bmc Neurology
Yi, Xingyang X; Wang, Chun C; Zhou, Qiang Q; Lin, Jing J
Publication Date: 2017-01-09

Variant appearance in text: rs2317676
PubMed Link: 28068952
Variant Present in the following documents:
  • Main text
  • 12883_2016_Article_788.pdf
View BVdb publication page



Incorporating epistasis interaction of genetic susceptibility single nucleotide polymorphisms in a lung cancer risk prediction model.

International Journal Of Oncology
Marcus, Michael W MW; Raji, Olaide Y OY; Duffy, Stephen W SW; Young, Robert P RP; Hopkins, Raewyn J RJ; Field, John K JK
Publication Date: 2016-07

Variant appearance in text: rs2317676
PubMed Link: 27121382
Variant Present in the following documents:
  • Main text
  • ijo-49-01-0361.pdf
View BVdb publication page



Genetic variation of ITGB3 is associated with asthma in Chinese Han children.

Plos One
Zhang, Yan Y; Han, Yuling Y; Dong, Liang L; Yu, Huafeng H; Cheng, Lu L; Zhao, Xiuxia X; Ding, Mingjie M
Publication Date: 2013

Variant appearance in text: rs2317676
PubMed Link: 23451109
Variant Present in the following documents:
  • Main text
  • pone.0056914.pdf
View BVdb publication page



Lung cancer susceptibility model based on age, family history and genetic variants.

Plos One
Young, Robert P RP; Hopkins, Raewyn J RJ; Hay, Bryan A BA; Epton, Michael J MJ; Mills, Graham D GD; Black, Peter N PN; Gardner, Heather D HD; Sullivan, Richard R; Gamble, Gregory D GD
Publication Date: 2009

Variant appearance in text: rs2317676
PubMed Link: 19390575
Variant Present in the following documents:
  • Main text
  • pone.0005302.pdf
View BVdb publication page



Assessing the reproducibility of asthma candidate gene associations, using genome-wide data.

American Journal Of Respiratory And Critical Care Medicine
Rogers, Angela J AJ; Raby, Benjamin A BA; Lasky-Su, Jessica A JA; Murphy, Amy A; Lazarus, Ross R; Klanderman, Barbara J BJ; Sylvia, Jody S JS; Ziniti, John P JP; Lange, Christoph C; Celedón, Juan C JC; Silverman, Edwin K EK; Weiss, Scott T ST
Publication Date: 2009-06-15

Variant appearance in text: rs2317676
PubMed Link: 19264973
Variant Present in the following documents:
  • Main text
View BVdb publication page



Variation in ITGB3 is associated with asthma and sensitization to mold allergen in four populations.

American Journal Of Respiratory And Critical Care Medicine
Weiss, Lauren A LA; Lester, Lucille A LA; Gern, James E JE; Wolf, Raoul L RL; Parry, Rodney R; Lemanske, Robert F RF; Solway, Julian J; Ober, Carole C
Publication Date: 2005-07-01

Variant appearance in text: rs2317676
PubMed Link: 15817799
Variant Present in the following documents:
  • Main text
View BVdb publication page