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CSF2RB c.1153-329A>T
Variant ID: 22-37329545-A-T
NM_000395.2(
CSF2RB
):c.1153-329A>T
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genome-wide discovery of genetic variants affecting tamoxifen sensitivity and their clinical and functional validation.
Annals Of Oncology : Official Journal Of The European Society For Medical Oncology
Weng, L L; Ziliak, D D; Im, H K HK; Gamazon, E R ER; Philips, S S; Nguyen, A T AT; Desta, Z Z; Skaar, T C TC; Flockhart, D A DA; Huang, R S RS; ,
Publication Date: 2013-07
Variant appearance in text: rs1534882
PubMed Link:
23508821
Variant Present in the following documents:
Main text
View BVdb publication page