MOESM3 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/MOESM3_of_PGG_SNV_understanding_the_evolutionary_and_medical_implications_of_human_single_nucleotide_variations_in_diverse_populations/10027907/1
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Additional file 3: Table S2. The list of Mendelian-inherited disease variants with alternative allele frequency larger than 0.05 in PGG.SNV.
补充材料3：表S2。PGG.SNV中替代等位基因频率（alternative allele frequency）大于0.05的孟德尔遗传病变异列表。
提供机构：
Xue, Zhe; Tian, Lei; Zhang, Chao; Yuan, Kai; Wang, Yuchen; Gao, Yang; Liu, Chang; Ning, Zhilin; Liu, Jiaojiao; Wang, Xiaoji; Lu, Dongsheng; Xu, Shuhua; Ge, Xueling; Xie, Bo; Lu, Yan; Hoh, Boon-Peng; Pan, Yuwen; Zhang, Xiaoxi
创建时间：
2019-10-23
