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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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