Additional file 2 of Evaluation and limitations of different approaches among COVID-19 fatal cases using whole-exome sequencing data

Additional file 2: Table S2. All 900 Covid-19 associated risk variants used in our analyses with Fisher's exact test p-values. • /p-value - included in the analysis; sig - significance: * - p-value < 0.05, ** - significant after Bonferroni correction; # - overlap with risk variants from QCI infection group; § - overlap with risk variants from QCI critical group; sN - Slovak NIPT data, W - WES data of Slovak dead patients, N - non-Finnish European gnomAD data.