PROCR c.323-207G>A

Variant ID: 20-33763764-G-A

NM_006404.4(PROCR):c.323-207G>A

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Large-Scale Targeted Sequencing Study of Ischemic Stroke in the Han Chinese Population.

Journal Of The American Heart Association
Shi, Mengyao M; Kelly, Tanika N TN; Zhu, Zhengbao Z; Li, Changwei C; Shen, Chong C; Sun, Yingxian Y; Wang, Aili A; Shan, Guangliang G; Bu, Xiaoqing X; Guo, Daoxia D; Zhao, Jingbo J; Xu, Tan T; Peng, Hao H; Xu, Tian T; Zhong, Chongke C; Sun, Xiao X; Chen, Jing J; Zhang, Yonghong Y; He, Jiang J
Publication Date: 2022-10-04

Variant appearance in text: rs2069951
PubMed Link: 36193932
Variant Present in the following documents:
  • JAH3-11-e025245.pdf
View BVdb publication page



Common Risk Factors Add to Inherited Thrombophilia to Predict Venous Thromboembolism Risk in Families.

Th Open : Companion Journal To Thrombosis And Haemostasis
Suchon, Pierre P; Resseguier, Noemie N; Ibrahim, Manal M; Robin, Alexia A; Venton, Geoffroy G; Barthet, Marie-Christine MC; Brunet, Dominique D; Saut, Noemie N; Alessi, Marie-Christine MC; Trégouët, David A DA; Morange, Pierre E PE
Publication Date: 2019-01

Variant appearance in text: rs2069951
PubMed Link: 31249979
Variant Present in the following documents:
  • Main text
  • 10-1055-s-0039-1677807.pdf
View BVdb publication page



Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke.

Plos One
Cole, John W JW; Xu, Huichun H; Ryan, Kathleen K; Jaworek, Thomas T; Dueker, Nicole N; McArdle, Patrick P; Gaynor, Brady B; Cheng, Yu-Ching YC; O'Connell, Jeffrey J; Bevan, Steve S; Malik, Rainer R; Ahmed, Naveed Uddin NU; Amouyel, Philippe P; Anjum, Sheraz S; Bis, Joshua C JC; Crosslin, David D; Danesh, John J; Engelter, Stefan T ST; Fornage, Myriam M; Frossard, Philippe P; Gieger, Christian C; Giese, Anne-Katrin AK; Grond-Ginsbach, Caspar C; Ho, Weang Kee WK; Holliday, Elizabeth E; Hopewell, Jemma J; Hussain, M M; Iqbal, W W; Jabeen, S S; Jannes, Jim J; Kamal, Ayeesha A; Kamatani, Yoichiro Y; Kanse, Sandip S; Kloss, Manja M; Lathrop, Mark M; Leys, Didier D; Lindgren, Arne A; Longstreth, W T WT; Mahmood, Khalid K; Meisinger, Christa C; Metso, Tiina M TM; Mosley, Thomas T; Müller-Nurasyid, Martina M; Norrving, Bo B; Parati, Eugenio E; Peters, Annette A; Pezzini, Alessandro A; Quereshi, I I; Rasheed, Asif A; Rauf, A A; Salam, T T; Shen, Jess J; Słowik, Agnieszka A; Stanne, Tara T; Strauch, Konstantin K; Tatlisumak, Turgut T; Thijs, Vincent N VN; Tiedt, Steffen S; Traylor, Matthew M; Waldenberger, Melanie M; Walters, Matthew M; Zhao, Wei W; Boncoraglio, Giorgio G; Debette, Stéphanie S; Jern, Christina C; Levi, Christopher C; Markus, Hugh H; Meschia, James J; Rolfs, Arndt A; Rothwell, Peter P; Saleheen, Danish D; Seshadri, Sudha S; Sharma, Pankaj P; Sudlow, Cathie C; Worrall, Bradford B; , ; , ; Stine, O Colin OC; Kittner, Steven J SJ; Mitchell, Braxton D BD
Publication Date: 2018

Variant appearance in text: rs2069951
PubMed Link: 30383853
Variant Present in the following documents:
  • Main text
View BVdb publication page



Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes.

Journal Of Thrombosis And Haemostasis : Jth
de Haan, H G HG; van Hylckama Vlieg, A A; Lotta, L A LA; Gorski, M M MM; Bucciarelli, P P; Martinelli, I I; Baglin, T P TP; Peyvandi, F F; Rosendaal, F R FR; ,
Publication Date: 2018-12

Variant appearance in text: rs2069951
PubMed Link: 30168256
Variant Present in the following documents:
  • NIHMS1021906-supplement-1.pdf
View BVdb publication page



Association of common genetic variation in the protein C pathway genes with clinical outcomes in acute respiratory distress syndrome.

Critical Care (London, England)
Sapru, Anil A; Liu, Kathleen D KD; Wiemels, Joseph J; Hansen, Helen H; Pawlikowska, Ludmilla L; Poon, Annie A; Jorgenson, Eric E; Witte, John S JS; Calfee, Carolyn S CS; Ware, Lorraine B LB; Matthay, Michael A MA; ,
Publication Date: 2016-05-23

Variant appearance in text: rs2069951
PubMed Link: 27215212
Variant Present in the following documents:
  • Main text
  • 13054_2016_Article_1330.pdf
View BVdb publication page



Single nucleotide variants in the protein C pathway and mortality in dialysis patients.

Plos One
Ocak, Gürbey G; Drechsler, Christiane C; Vossen, Carla Y CY; Vos, Hans L HL; Rosendaal, Frits R FR; Reitsma, Pieter H PH; Hoffmann, Michael M MM; März, Winfried W; Ouwehand, Willem H WH; Krediet, Raymond T RT; Boeschoten, Elisabeth W EW; Dekker, Friedo W FW; Wanner, Christoph C; Verduijn, Marion M
Publication Date: 2014

Variant appearance in text: rs2069951
PubMed Link: 24816905
Variant Present in the following documents:
  • Main text
  • pone.0097251.pdf
View BVdb publication page