Supplementary Table S2 from A Heritable Missense Polymorphism in <i>CDKN2A</i> Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal Evolution

Kyle M. Walsh,Adam J. de Smith,Helen M. Hansen,Ivan V. Smirnov,Semira Gonseth,Alyson A. Endicott,Jianqiao Xiao,Terri Rice,Cecilia H. Fu,Lucie S. McCoy,Daniel H. Lachance,Jeanette E. Eckel-Passow,John K. Wiencke,Robert B. Jenkins,Margaret R. Wrensch,Xiaomei Ma,Catherine Metayer,Joseph L. Wiemels

crossref（2023）

Cited 0|Views12

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Abstract

Top SNP associations in the 9p21.3 region evaluated in Hispanic ALL patients from CCLS and validated in European-ancestry ALL patients from COG, with functional annotation.

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Supplementary Table S2 from A Heritable Missense Polymorphism in &lt;i&gt;CDKN2A&lt;/i&gt; Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal Evolution

Supplementary Table S2 from A Heritable Missense Polymorphism in <i>CDKN2A</i> Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal Evolution