EPHX1 c.365-1558T>C

Variant ID: 1-226024797-T-C

NM_001136018.2(EPHX1):c.365-1558T>C

This variant was identified in 8 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: rs2740170
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Candidate gene linkage approach to identify DNA variants that predispose to preterm birth.

Pediatric Research
Bream, Elise N A EN; Leppellere, Cara R CR; Cooper, Margaret E ME; Dagle, John M JM; Merrill, David C DC; Christensen, Kaare K; Simhan, Hyagriv N HN; Fong, Chin-To CT; Hallman, Mikko M; Muglia, Louis J LJ; Marazita, Mary L ML; Murray, Jeffrey C JC
Publication Date: 2013-02

Variant appearance in text: rs2740170
PubMed Link: 23168575
Variant Present in the following documents:
  • Main text
View BVdb publication page



Pharmacogenomics of warfarin in populations of African descent.

British Journal Of Clinical Pharmacology
Suarez-Kurtz, Guilherme G; Botton, Mariana R MR
Publication Date: 2013-02

Variant appearance in text: rs2740170
PubMed Link: 22676711
Variant Present in the following documents:
  • Main text
View BVdb publication page



Impact of interactions of cigarette smoking with NAT2 polymorphisms on rheumatoid arthritis risk in African Americans.

Arthritis And Rheumatism
Mikuls, Ted R TR; Levan, Tricia T; Gould, Karen A KA; Yu, Fang F; Thiele, Geoffrey M GM; Bynote, Kimberly K KK; Conn, Doyt D; Jonas, Beth L BL; Callahan, Leigh F LF; Smith, Edwin E; Brasington, Richard R; Moreland, Larry W LW; Reynolds, Richard R; Gaffo, Angelo A; Bridges, S Louis SL
Publication Date: 2012-03

Variant appearance in text: rs2740170
PubMed Link: 21989592
Variant Present in the following documents:
  • Main text
View BVdb publication page



New genetic variant that might improve warfarin dose prediction in African Americans.

British Journal Of Clinical Pharmacology
Schelleman, Hedi H; Brensinger, Colleen M CM; Chen, Jinbo J; Finkelman, Brian S BS; Rieder, Mark J MJ; Kimmel, Stephen E SE
Publication Date: 2010-09

Variant appearance in text: rs2740170
PubMed Link: 20716240
Variant Present in the following documents:
  • Main text
View BVdb publication page



Evaluation of candidate genes in a genome-wide association study of childhood asthma in Mexicans.

The Journal Of Allergy And Clinical Immunology
Wu, Hao H; Romieu, Isabelle I; Shi, Min M; Hancock, Dana B DB; Li, Huiling H; Sienra-Monge, Juan-Jose JJ; Chiu, Grace Y GY; Xu, Hong H; del Rio-Navarro, Blanca Estela BE; London, Stephanie J SJ
Publication Date: 2010-02

Variant appearance in text: rs2740170
PubMed Link: 19910030
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic associations with hypoxemia and pulmonary arterial pressure in COPD.

Chest
Castaldi, Peter J PJ; Hersh, Craig P CP; Reilly, John J JJ; Silverman, Edwin K EK
Publication Date: 2009-03

Variant appearance in text: rs2740170
PubMed Link: 19017876
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of warfarin dose with genes involved in its action and metabolism.

Human Genetics
Wadelius, Mia M; Chen, Leslie Y LY; Eriksson, Niclas N; Bumpstead, Suzannah S; Ghori, Jilur J; Wadelius, Claes C; Bentley, David D; McGinnis, Ralph R; Deloukas, Panos P
Publication Date: 2007-03

Variant appearance in text: rs2740170
PubMed Link: 17048007
Variant Present in the following documents:
View BVdb publication page