Additional file 2: Table S1. of Pathogenic variant burden in the ExAC database: an empirical approach to evaluating population data for clinical variant interpretation
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https://figshare.com/articles/dataset/Additional_file_2_Table_S1_of_Pathogenic_variant_burden_in_the_ExAC_database_an_empirical_approach_to_evaluating_population_data_for_clinical_variant_interpretation/4625437
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资源简介：
List of the all NMDpositive variants with allele frequencies greater than 0.01% in the set of genes described in Table 2. Known and suspected founder mutations are indicated. PCD primary ciliary dyskinesia. (XLSX 48 kb)
创建时间：
2017-02-07
