Additional file 1 of Enhanced rare disease mapping for phenome-wide genetic association in the UK Biobank
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https://springernature.figshare.com/articles/dataset/Additional_file_1_of_Enhanced_rare_disease_mapping_for_phenome-wide_genetic_association_in_the_UK_Biobank/20461969/1
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Additional file 1: Table S1: ICD-10 code to Orpha code consensus mapping. Table S2: Sample sizes and demographics obtained for rare disorders. Table S4: Significantly comorbid rare disease pairs (Bonferroni adjustment). Table S5: Complex diseases significantly comorbid with rare diseases (Bonferroni adjustment). Table S7: Significant gene-level associations (FDR<=0.05). Table S8: Significant variant-level associations (FDR<=0.05).
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figshare
创建时间：
2022-08-10
