Table S2
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<b>Table S2.</b> SNP identification (Marker) and progressive number (N°), allelic variants (SNP), lines carrying each allelic variant (OBS), additive effect and significance values for the association between the SNP and the phenotype (P-value and RMIP) and proportion of the phenotypic variance explained by the SNP (R<sup>2</sup>).
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figshare
创建时间：
2018-12-20
