MOESM5 of PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations
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https://springernature.figshare.com/articles/dataset/MOESM5_of_PGG_SNV_understanding_the_evolutionary_and_medical_implications_of_human_single_nucleotide_variations_in_diverse_populations/10027922/1
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Additional file 5: Table S4. The list of Mendelian-inherited disease variants showing large differentiation between ancestries (DiffAnces > 0.1).
提供机构：
figshare
创建时间：
2019-10-23
