MOESM3 of PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations
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https://figshare.com/articles/dataset/MOESM3_of_PGG_SNV_understanding_the_evolutionary_and_medical_implications_of_human_single_nucleotide_variations_in_diverse_populations/10027907
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资源简介：
Additional file 3: Table S2. The list of Mendelian-inherited disease variants with alternative allele frequency larger than 0.05 in PGG.SNV.
创建时间：
2019-10-22
