ABCC2 c.3414+437G>A

Variant ID: 10-101594729-G-A

NM_000392.3(ABCC2):c.3414+437G>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2.

European Journal Of Human Genetics : Ejhg
Slachtova, Lenka L; Seda, Ondrej O; Behunova, Jana J; Mistrik, Martin M; Martasek, Pavel P
Publication Date: 2016-05

Variant appearance in text: rs7476245
PubMed Link: 26350512
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: rs7476245
PubMed Link: 22454423
Variant Present in the following documents:
  • Main text
View BVdb publication page



Analysis of pharmacogenetic traits in two distinct South African populations.

Human Genomics
Ikediobi, Ogechi O; Aouizerat, Bradley B; Xiao, Yuanyuan Y; Gandhi, Monica M; Gebhardt, Stefan S; Warnich, Louise L
Publication Date: 2011-05

Variant appearance in text: rs7476245
PubMed Link: 21712189
Variant Present in the following documents:
  • Main text
View BVdb publication page