CETP c.981+706T>A

Variant ID: 16-57009769-T-A

NM_000078.2(CETP):c.981+706T>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


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: rs736274
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Multiple linear combination (MLC) regression tests for common variants adapted to linkage disequilibrium structure.

Genetic Epidemiology
Yoo, Yun Joo YJ; Sun, Lei L; Poirier, Julia G JG; Paterson, Andrew D AD; Bull, Shelley B SB
Publication Date: 2017-02

Variant appearance in text: rs736274
PubMed Link: 27885705
Variant Present in the following documents:
  • Main text
  • GEPI-41-108.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: rs736274
PubMed Link: 14707174
Variant Present in the following documents:
  • Main text
View BVdb publication page