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.




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
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