GCLC c.753+2354G>T

Variant ID: 6-53376648-C-A

NM_001498.3(GCLC):c.753+2354G>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways.

Birth Defects Research. Part A, Clinical And Molecular Teratology
Hobbs, Charlotte A CA; Cleves, Mario A MA; Macleod, Stewart L SL; Erickson, Stephen W SW; Tang, Xinyu X; Li, Jingyun J; Li, Ming M; Nick, Todd T; Malik, Sadia S; ,
Publication Date: 2014-02

Variant appearance in text: rs542914
PubMed Link: 24535845
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variations and patient-reported quality of life among patients with lung cancer.

Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology
Sloan, Jeff A JA; de Andrade, Mariza M; Decker, Paul P; Wampfler, Jason J; Oswold, Curtis C; Clark, Matthew M; Yang, Ping P
Publication Date: 2012-05-10

Variant appearance in text: rs542914
PubMed Link: 22454423
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variants associated with the risk of chronic obstructive pulmonary disease with and without lung cancer.

Cancer Prevention Research (Philadelphia, Pa.)
de Andrade, Mariza M; Li, Yan Y; Marks, Randolph S RS; Deschamps, Claude C; Scanlon, Paul D PD; Olswold, Curtis L CL; Jiang, Ruoxiang R; Swensen, Stephen J SJ; Sun, Zhifu Z; Cunningham, Julie M JM; Wampfler, Jason A JA; Limper, Andrew H AH; Midthun, David E DE; Yang, Ping P
Publication Date: 2012-03

Variant appearance in text: rs542914
PubMed Link: 22044695
Variant Present in the following documents:
  • Main text
View BVdb publication page