CETP c.930+312A>T

Variant ID: 16-57007734-A-T

NM_000078.2(CETP):c.930+312A>T

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Cholesteryl ester transfer protein (CETP) as a drug target for cardiovascular disease.

Nature Communications
Schmidt, Amand F AF; Hunt, Nicholas B NB; Gordillo-Marañón, Maria M; Charoen, Pimphen P; Drenos, Fotios F; Kivimaki, Mika M; Lawlor, Deborah A DA; Giambartolomei, Claudia C; Papacosta, Olia O; Chaturvedi, Nishi N; Bis, Joshua C JC; O'Donnell, Christopher J CJ; Wannamethee, Goya G; Wong, Andrew A; Price, Jackie F JF; Hughes, Alun D AD; Gaunt, Tom R TR; Franceschini, Nora N; Mook-Kanamori, Dennis O DO; Zwierzyna, Magdalena M; Sofat, Reecha R; Hingorani, Aroon D AD; Finan, Chris C
Publication Date: 2021-09-24

Variant appearance in text: rs158478
PubMed Link: 34561430
Variant Present in the following documents:
  • 41467_2021_25703_MOESM1_ESM.pdf
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Candidate Gene Analysis Reveals Strong Association of CETP Variants With High Density Lipoprotein Cholesterol and PCSK9 Variants With Low Density Lipoprotein Cholesterol in Ghanaian Adults: An AWI-Gen Sub-Study.

Frontiers In Genetics
Agongo, Godfred G; Amenga-Etego, Lucas L; Nonterah, Engelbert A EA; Debpuur, Cornelius C; Choudhury, Ananyo A; Bentley, Amy R AR; Oduro, Abraham R AR; Rotimi, Charles N CN; Crowther, Nigel J NJ; Ramsay, Michèle M; , ; H Africa,
Publication Date: 2020

Variant appearance in text: rs158478
PubMed Link: 33193594
Variant Present in the following documents:
  • Main text
  • fgene-11-456661.pdf
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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs158478
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Genetic variants in CETP increase risk of intracerebral hemorrhage.

Annals Of Neurology
Anderson, Christopher D CD; Falcone, Guido J GJ; Phuah, Chia-Ling CL; Radmanesh, Farid F; Brouwers, H Bart HB; Battey, Thomas W K TW; Biffi, Alessandro A; Peloso, Gina M GM; Liu, Dajiang J DJ; Ayres, Alison M AM; Goldstein, Joshua N JN; Viswanathan, Anand A; Greenberg, Steven M SM; Selim, Magdy M; Meschia, James F JF; Brown, Devin L DL; Worrall, Bradford B BB; Silliman, Scott L SL; Tirschwell, David L DL; Flaherty, Matthew L ML; Kraft, Peter P; Jagiella, Jeremiasz M JM; Schmidt, Helena H; Hansen, Björn M BM; Jimenez-Conde, Jordi J; Giralt-Steinhauer, Eva E; Elosua, Roberto R; Cuadrado-Godia, Elisa E; Soriano, Carolina C; van Nieuwenhuizen, Koen M KM; Klijn, Catharina J M CJ; Rannikmae, Kristiina K; Samarasekera, Neshika N; Al-Shahi Salman, Rustam R; Sudlow, Catherine L CL; Deary, Ian J IJ; Morotti, Andrea A; Pezzini, Alessandro A; Pera, Joanna J; Urbanik, Andrzej A; Pichler, Alexander A; Enzinger, Christian C; Norrving, Bo B; Montaner, Joan J; Fernandez-Cadenas, Israel I; Delgado, Pilar P; Roquer, Jaume J; Lindgren, Arne A; Slowik, Agnieszka A; Schmidt, Reinhold R; Kidwell, Chelsea S CS; Kittner, Steven J SJ; Waddy, Salina P SP; Langefeld, Carl D CD; Abecasis, Goncalo G; Willer, Cristen J CJ; Kathiresan, Sekar S; Woo, Daniel D; Rosand, Jonathan J; ,
Publication Date: 2016-11

Variant appearance in text: rs158478
PubMed Link: 27717122
Variant Present in the following documents:
  • Main text
  • ANA-80-730.pdf
View BVdb publication page



High-throughput MALDI-TOF discovery of genomic sequence polymorphisms.

Genome Research
Stanssens, Patrick P; Zabeau, Marc M; Meersseman, Geert G; Remes, Gwen G; Gansemans, Yannick Y; Storm, Niels N; Hartmer, Ralf R; Honisch, Christiane C; Rodi, Charles P CP; Böcker, Sebastian S; van den Boom, Dirk D
Publication Date: 2004-01

Variant appearance in text: rs158478
PubMed Link: 14707174
Variant Present in the following documents:
  • Main text
View BVdb publication page