13059_2019_1838_MOESM3_ESM.xlsx (29.43 MB)
MOESM3 of PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations
dataset
posted on 2019-10-23, 08:27 authored by Chao Zhang, Yang Gao, Zhilin Ning, Yan Lu, Xiaoxi Zhang, Jiaojiao Liu, Bo Xie, Zhe Xue, Xiaoji Wang, Kai Yuan, Xueling Ge, Yuwen Pan, Chang Liu, Lei Tian, Yuchen Wang, Dongsheng Lu, Boon-Peng Hoh, Shuhua XuAdditional file 3: Table S2. The list of Mendelian-inherited disease variants with alternative allele frequency larger than 0.05 in PGG.SNV.
