Summary of significant mtSNPs.
收藏NIAID Data Ecosystem2026-03-08 收录
下载链接：
https://figshare.com/articles/dataset/_Summary_of_significant_mtSNPs_/1406875
下载链接
链接失效反馈官方服务：
资源简介：
Genomic position in base pairs (bp), alleles, rs_number, and point mutation are based on the NCBI dbSNP GRCh38 human genome assembly (rCRS, GeneBank ID J01415.2). Alleles are given in terms of major→minor allele. The population minor allele frequency “maf” is based on 2,704 individuals provided by mitomap (http://www.mitomap.org). Note that these allele frequency estimates do not account for the presence of heteroplasmy. An estimated effect size (βSNP) < 0 indicates that the risk allele is the minor allele. Nominal p-values and adjusted p-values are provided. mtSNPs mt3336, mt5285 and mt14000 are also included in other chips.
Summary of significant mtSNPs.
创建时间：
2015-05-06
