BAZ1B c.3249+86A>G

Variant ID: 7-72877166-T-C

NM_032408.3(BAZ1B):c.3249+86A>G

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Integrated proteogenomic characterization across major histological types of pituitary neuroendocrine tumors.

Cell Research
Zhang, Fan F; Zhang, Qilin Q; Zhu, Jiajun J; Yao, Boyuan B; Ma, Chi C; Qiao, Nidan N; He, Shiman S; Ye, Zhao Z; Wang, Yunzhi Y; Han, Rui R; Feng, Jinwen J; Wang, Yongfei Y; Qin, Zhaoyu Z; Ma, Zengyi Z; Li, Kai K; Zhang, Yichao Y; Tian, Sha S; Chen, Zhengyuan Z; Tan, Subei S; Wu, Yue Y; Ran, Peng P; Wang, Ye Y; Ding, Chen C; Zhao, Yao Y
Publication Date: 2022-12

Variant appearance in text: rs2074755
PubMed Link: 36307579
Variant Present in the following documents:
  • 41422_2022_736_MOESM10_ESM.xlsx, sheet 3
View BVdb publication page



Trimethylamine N-oxide and its precursors in relation to blood pressure: A mendelian randomization study.

Frontiers In Cardiovascular Medicine
Wang, Han H; Luo, Qiang Q; Ding, Xunshi X; Chen, Lifang L; Zhang, Zheng Z
Publication Date: 2022

Variant appearance in text: rs2074755
PubMed Link: 35935641
Variant Present in the following documents:
  • Main text
  • fcvm-09-922441.pdf
View BVdb publication page



Systemic Investigation of Promoter-wide Methylome and Genome Variations in Gout.

International Journal Of Molecular Sciences
Tseng, Chia-Chun CC; Wong, Man Chun MC; Liao, Wei-Ting WT; Chen, Chung-Jen CJ; Lee, Su-Chen SC; Yen, Jeng-Hsien JH; Chang, Shun-Jen SJ
Publication Date: 2020-07-01

Variant appearance in text: rs2074755
PubMed Link: 32630231
Variant Present in the following documents:
  • ijms-21-04702-s001.pdf
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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: BAZ1B: 3249+86A>G; rs2074755
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
View BVdb publication page



Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration.

European Heart Journal
Angelakopoulou, Aspasia A; Shah, Tina T; Sofat, Reecha R; Shah, Sonia S; Berry, Diane J DJ; Cooper, Jackie J; Palmen, Jutta J; Tzoulaki, Ioanna I; Wong, Andrew A; Jefferis, Barbara J BJ; Maniatis, Nikolas N; Drenos, Fotios F; Gigante, Bruna B; Hardy, Rebecca R; Laxton, Ross C RC; Leander, Karin K; Motterle, Anna A; Simpson, Iain A IA; Smeeth, Liam L; Thomson, Andy A; Verzilli, Claudio C; Kuh, Diana D; Ireland, Helen H; Deanfield, John J; Caulfield, Mark M; Wallace, Chris C; Samani, Nilesh N; Munroe, Patricia B PB; Lathrop, Mark M; Fowkes, F Gerry R FG; Marmot, Michael M; Whincup, Peter H PH; Whittaker, John C JC; de Faire, Ulf U; Kivimaki, Mika M; Kumari, Meena M; Hypponen, Elina E; Power, Chris C; Humphries, Steve E SE; Talmud, Philippa J PJ; Price, Jackie J; Morris, Richard W RW; Ye, Shu S; Casas, Juan P JP; Hingorani, Aroon D AD
Publication Date: 2012-02

Variant appearance in text: rs2074755
PubMed Link: 21804106
Variant Present in the following documents:
  • Main text
  • ehr225.pdf
View BVdb publication page



Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.

Plos One
Zeller, Tanja T; Wild, Philipp P; Szymczak, Silke S; Rotival, Maxime M; Schillert, Arne A; Castagne, Raphaele R; Maouche, Seraya S; Germain, Marine M; Lackner, Karl K; Rossmann, Heidi H; Eleftheriadis, Medea M; Sinning, Christoph R CR; Schnabel, Renate B RB; Lubos, Edith E; Mennerich, Detlev D; Rust, Werner W; Perret, Claire C; Proust, Carole C; Nicaud, Viviane V; Loscalzo, Joseph J; Hübner, Norbert N; Tregouet, David D; Münzel, Thomas T; Ziegler, Andreas A; Tiret, Laurence L; Blankenberg, Stefan S; Cambien, François F
Publication Date: 2010-05-18

Variant appearance in text: rs2074755
PubMed Link: 20502693
Variant Present in the following documents:
  • Main text
View BVdb publication page



Evaluation of genetic risk scores for lipid levels using genome-wide markers in the Framingham Heart Study.

Bmc Proceedings
Piccolo, Stephen R SR; Abo, Ryan P RP; Allen-Brady, Kristina K; Camp, Nicola J NJ; Knight, Stacey S; Anderson, Jeffrey L JL; Horne, Benjamin D BD
Publication Date: 2009-12-15

Variant appearance in text: rs2074755
PubMed Link: 20018038
Variant Present in the following documents:
  • Main text
View BVdb publication page



A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia.

Human Molecular Genetics
Hegele, Robert A RA; Ban, Matthew R MR; Hsueh, Neil N; Kennedy, Brooke A BA; Cao, Henian H; Zou, Guang Yong GY; Anand, Sonia S; Yusuf, Salim S; Huff, Murray W MW; Wang, Jian J
Publication Date: 2009-11-01

Variant appearance in text: rs2074755
PubMed Link: 19656773
Variant Present in the following documents:
  • Main text
  • ddp361_1.pdf
  • ddp361.pdf
View BVdb publication page



Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.

American Journal Of Human Genetics
Wallace, Chris C; Newhouse, Stephen J SJ; Braund, Peter P; Zhang, Feng F; Tobin, Martin M; Falchi, Mario M; Ahmadi, Kourosh K; Dobson, Richard J RJ; Marçano, Ana Carolina B AC; Hajat, Cother C; Burton, Paul P; Deloukas, Panagiotis P; Brown, Morris M; Connell, John M JM; Dominiczak, Anna A; Lathrop, G Mark GM; Webster, John J; Farrall, Martin M; Spector, Tim T; Samani, Nilesh J NJ; Caulfield, Mark J MJ; Munroe, Patricia B PB
Publication Date: 2008-01

Variant appearance in text: rs2074755
PubMed Link: 18179892
Variant Present in the following documents:
  • Main text
View BVdb publication page