MOESM3 of PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations
收藏DataCite Commons2024-02-07 更新2024-07-27 收录
下载链接：
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
下载链接
链接失效反馈官方服务：
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.
提供机构：
figshare
创建时间：
2019-10-23
