CASZ1 c.-77+24211C>A

Variant ID: 1-10796547-G-T

NM_001079843.3(CASZ1):c.-77+24211C>A

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction.

Nature Genetics
Miyazawa, Kazuo K; Ito, Kaoru K; Ito, Masamichi M; Zou, Zhaonan Z; Kubota, Masayuki M; Nomura, Seitaro S; Matsunaga, Hiroshi H; Koyama, Satoshi S; Ieki, Hirotaka H; Akiyama, Masato M; Koike, Yoshinao Y; Kurosawa, Ryo R; Yoshida, Hiroki H; Ozaki, Kouichi K; Onouchi, Yoshihiro Y; , ; Takahashi, Atsushi A; Matsuda, Koichi K; Murakami, Yoshinori Y; Aburatani, Hiroyuki H; Kubo, Michiaki M; Momozawa, Yukihide Y; Terao, Chikashi C; Oki, Shinya S; Akazawa, Hiroshi H; Kamatani, Yoichiro Y; Komuro, Issei I
Publication Date: 2023-01-19

Variant appearance in text: rs17035646
PubMed Link: 36653681
Variant Present in the following documents:
  • 41588_2022_1284_MOESM3_ESM.pdf
View BVdb publication page



Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.

Nature Communications
Georges, Adrien A; Yang, Min-Lee ML; Berrandou, Takiy-Eddine TE; Bakker, Mark K MK; Dikilitas, Ozan O; Kiando, Soto Romuald SR; Ma, Lijiang L; Satterfield, Benjamin A BA; Sengupta, Sebanti S; Yu, Mengyao M; Deleuze, Jean-François JF; Dupré, Delia D; Hunker, Kristina L KL; Kyryachenko, Sergiy S; Liu, Lu L; Sayoud-Sadeg, Ines I; Amar, Laurence L; Brummett, Chad M CM; Coleman, Dawn M DM; d'Escamard, Valentina V; de Leeuw, Peter P; Fendrikova-Mahlay, Natalia N; Kadian-Dodov, Daniella D; Li, Jun Z JZ; Lorthioir, Aurélien A; Pappaccogli, Marco M; Prejbisz, Aleksander A; Smigielski, Witold W; Stanley, James C JC; Zawistowski, Matthew M; Zhou, Xiang X; Zöllner, Sebastian S; , ; , ; , ; Amouyel, Philippe P; De Buyzere, Marc L ML; Debette, Stéphanie S; Dobrowolski, Piotr P; Drygas, Wojciech W; Gornik, Heather L HL; Olin, Jeffrey W JW; Piwonski, Jerzy J; Rietzschel, Ernst R ER; Ruigrok, Ynte M YM; Vikkula, Miikka M; Warchol Celinska, Ewa E; Januszewicz, Andrzej A; Kullo, Iftikhar J IJ; Azizi, Michel M; Jeunemaitre, Xavier X; Persu, Alexandre A; Kovacic, Jason C JC; Ganesh, Santhi K SK; Bouatia-Naji, Nabila N
Publication Date: 2021-10-15

Variant appearance in text: rs17035646
PubMed Link: 34654805
Variant Present in the following documents:
  • 41467_2021_26174_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.

Nature Communications
Georges, Adrien A; Yang, Min-Lee ML; Berrandou, Takiy-Eddine TE; Bakker, Mark K MK; Dikilitas, Ozan O; Kiando, Soto Romuald SR; Ma, Lijiang L; Satterfield, Benjamin A BA; Sengupta, Sebanti S; Yu, Mengyao M; Deleuze, Jean-François JF; Dupré, Delia D; Hunker, Kristina L KL; Kyryachenko, Sergiy S; Liu, Lu L; Sayoud-Sadeg, Ines I; Amar, Laurence L; Brummett, Chad M CM; Coleman, Dawn M DM; d'Escamard, Valentina V; de Leeuw, Peter P; Fendrikova-Mahlay, Natalia N; Kadian-Dodov, Daniella D; Li, Jun Z JZ; Lorthioir, Aurélien A; Pappaccogli, Marco M; Prejbisz, Aleksander A; Smigielski, Witold W; Stanley, James C JC; Zawistowski, Matthew M; Zhou, Xiang X; Zöllner, Sebastian S; , ; , ; , ; Amouyel, Philippe P; De Buyzere, Marc L ML; Debette, Stéphanie S; Dobrowolski, Piotr P; Drygas, Wojciech W; Gornik, Heather L HL; Olin, Jeffrey W JW; Piwonski, Jerzy J; Rietzschel, Ernst R ER; Ruigrok, Ynte M YM; Vikkula, Miikka M; Warchol Celinska, Ewa E; Januszewicz, Andrzej A; Kullo, Iftikhar J IJ; Azizi, Michel M; , ; Jeunemaitre, Xavier X; Persu, Alexandre A; Kovacic, Jason C JC; Ganesh, Santhi K SK; Bouatia-Naji, Nabila N
Publication Date: 2021-10-15

Variant appearance in text: rs17035646
PubMed Link: 34654805
Variant Present in the following documents:
  • 41467_2021_26174_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group.

American Journal Of Hypertension
Irvin, Marguerite R MR; Sitlani, Colleen M CM; Floyd, James S JS; Psaty, Bruce M BM; Bis, Joshua C JC; Wiggins, Kerri L KL; Whitsel, Eric A EA; Sturmer, Til T; Stewart, James J; Raffield, Laura L; Sun, Fangui F; Liu, Ching-Ti CT; Xu, Hanfei H; Cupples, Adrienne L AL; Tanner, Rikki M RM; Rossing, Peter P; Smith, Albert A; Zilhão, Nuno R NR; Launer, Lenore J LJ; Noordam, Raymond R; Rotter, Jerome I JI; Yao, Jie J; Li, Xiaohui X; Guo, Xiuqing X; Limdi, Nita N; Sundaresan, Aishwarya A; Lange, Leslie L; Correa, Adolfo A; Stott, David J DJ; Ford, Ian I; Jukema, J Wouter JW; Gudnason, Vilmundur V; Mook-Kanamori, Dennis O DO; Trompet, Stella S; Palmas, Walter W; Warren, Helen R HR; Hellwege, Jacklyn N JN; Giri, Ayush A; O'donnell, Christopher C; Hung, Adriana M AM; Edwards, Todd L TL; Ahluwalia, Tarunveer S TS; Arnett, Donna K DK; Avery, Christy L CL
Publication Date: 2019-11-15

Variant appearance in text: rs17035646
PubMed Link: 31545351
Variant Present in the following documents:
  • Main text
View BVdb publication page