RRM1 c.1038+151C>G

Variant ID: 11-4143146-C-G

NM_001033.3(RRM1):c.1038+151C>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


RRM1 and RRM2 pharmacogenetics: association with phenotypes in HapMap cell lines and acute myeloid leukemia patients.

Pharmacogenomics
Cao, Xueyuan X; Mitra, Amit K AK; Pounds, Stanley S; Crews, Kristine R KR; Gandhi, Varsha V; Plunkett, William W; Dolan, M Eileen ME; Hartford, Christine C; Raimondi, Susana S; Campana, Dario D; Downing, James J; Rubnitz, Jeffrey E JE; Ribeiro, Raul C RC; Lamba, Jatinder K JK
Publication Date: 2013-09

Variant appearance in text: rs12288551
PubMed Link: 24024897
Variant Present in the following documents:
  • Main text
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