DPYD c.151-5723G>T

Variant ID: 1-98299475-C-A

NM_000110.3(DPYD):c.151-5723G>T

This variant was identified in 5 publications

View GRCh38 version.




Publications:


A Combined Transcriptomic and Genomic Analysis Identifies a Gene Signature Associated With the Response to Anti-TNF Therapy in Rheumatoid Arthritis.

Frontiers In Immunology
Aterido, Adrià A; Cañete, Juan D JD; Tornero, Jesús J; Blanco, Francisco F; Fernández-Gutierrez, Benjamín B; Pérez, Carolina C; Alperi-López, Mercedes M; Olivè, Alex A; Corominas, Héctor H; Martínez-Taboada, Víctor V; González, Isidoro I; Fernández-Nebro, Antonio A; Erra, Alba A; López-Lasanta, María M; López Corbeto, Mireia M; Palau, Núria N; Marsal, Sara S; Julià, Antonio A
Publication Date: 2019

Variant appearance in text: rs10747488
PubMed Link: 31312201
Variant Present in the following documents:
  • Main text
  • fimmu-10-01459.pdf
View BVdb publication page



Uncovering the complex genetics of human character.

Molecular Psychiatry
Zwir, Igor I; Arnedo, Javier J; Del-Val, Coral C; Pulkki-Råback, Laura L; Konte, Bettina B; Yang, Sarah S SS; Romero-Zaliz, Rocio R; Hintsanen, Mirka M; Cloninger, Kevin M KM; Garcia, Danilo D; Svrakic, Dragan M DM; Rozsa, Sandor S; Martinez, Maribel M; Lyytikäinen, Leo-Pekka LP; Giegling, Ina I; Kähönen, Mika M; Hernandez-Cuervo, Helena H; Seppälä, Ilkka I; Raitoharju, Emma E; de Erausquin, Gabriel A GA; Raitakari, Olli O; Rujescu, Dan D; Postolache, Teodor T TT; Sung, Joohon J; Keltikangas-Järvinen, Liisa L; Lehtimäki, Terho T; Cloninger, C Robert CR
Publication Date: 2020-10

Variant appearance in text: DPYD: 151-5723G>T; rs10747488
PubMed Link: 30283034
Variant Present in the following documents:
  • 41380_2018_263_MOESM14_ESM.xlsx, sheet 1
View BVdb publication page



Uncovering the complex genetics of human temperament.

Molecular Psychiatry
Zwir, Igor I; Arnedo, Javier J; Del-Val, Coral C; Pulkki-Råback, Laura L; Konte, Bettina B; Yang, Sarah S SS; Romero-Zaliz, Rocio R; Hintsanen, Mirka M; Cloninger, Kevin M KM; Garcia, Danilo D; Svrakic, Dragan M DM; Rozsa, Sandor S; Martinez, Maribel M; Lyytikäinen, Leo-Pekka LP; Giegling, Ina I; Kähönen, Mika M; Hernandez-Cuervo, Helena H; Seppälä, Ilkka I; Raitoharju, Emma E; de Erausquin, Gabriel A GA; Raitakari, Olli O; Rujescu, Dan D; Postolache, Teodor T TT; Sung, Joohon J; Keltikangas-Järvinen, Liisa L; Lehtimäki, Terho T; Cloninger, C Robert CR
Publication Date: 2020-10

Variant appearance in text: DPYD: 151-5723G>T; rs10747488
PubMed Link: 30279457
Variant Present in the following documents:
  • 41380_2018_264_MOESM15_ESM.xlsx, sheet 1
View BVdb publication page



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: rs10747488
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Item-level analyses reveal genetic heterogeneity in neuroticism.

Nature Communications
Nagel, Mats M; Watanabe, Kyoko K; Stringer, Sven S; Posthuma, Danielle D; van der Sluis, Sophie S
Publication Date: 2018-03-02

Variant appearance in text: rs10747488
PubMed Link: 29500382
Variant Present in the following documents:
  • 41467_2018_3242_MOESM2_ESM.pdf
View BVdb publication page